737 20 16481 Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Faculty Publications Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Creator An entity primarily responsible for making the resource TA, Augusty; DSouza, Greta Title A name given to the resource Validating a Teacher Professional Development Program to Develop Leadership and Mentorship among in-Service Teachers Date A point or period of time associated with an event in the lifecycle of the resource 01-01-2026 Source A related resource from which the described resource is derived International Journal of Educational Reform; Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1177/10567879261446919" target="_blank" rel="noreferrer noopener">https://doi.org/10.1177/10567879261446919</a> <a href="https://www.scopus.com/pages/publications/105038618338?origin=resultslist" target="_blank" rel="noreferrer noopener">https://www.scopus.com/pages/publications/105038618338?origin=resultslist</a> Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant TA A., School of Education, CHRIST University, Bangalore, India; DSouza G., School of Education, CHRIST University, Bangalore, India Description An account of the resource School teachers are pivotal in shaping the world's future. Their ongoing professional development (PD) is crucial to fostering a positive school culture. This study aimed to develop and validate a PD program for in-service teachers, ensuring its content and empirical validity in enhancing teacher leadership and mentorship. The module underwent content validation by 14 experts using Lawshe's content validity ratio and the content validity index to determine its appropriateness and alignment with PD proposed by the National Education Policy 2020. Empirical validation was conducted with 30 participants using a single-group pre-testpost-test design to measure the module's impact. Content validation confirmed the high expert agreement, indicating strong content relevance. Empirical validation revealed significant improvements in participants leadership and mentorship competencies as evidenced by positive post-test outcomes. The findings suggest that the module effectively enhances teacher professional development (TPD) by improving association, professional learning, assessment, instruction, community and policy in leadership, and self-efficacy and outcome expectancy in mentorship. The validated module is a structured framework for TPD that contributes to evidence-based educational training. Future research could explore its long-term effectiveness with larger samples and a mixed-methods design, employing multiple models and frameworks, including India-specific ones, across diverse educational contexts. The Author(s) 2026 Subject The topic of the resource content validity; empirical validity; leadership; mentorship; module development; professional development Publisher An entity responsible for making the resource available SAGE Publications Inc. Relation A related resource ISSN: 10567879; Language A language of the resource English Type The nature or genre of the resource Article Rights Information about rights held in and over the resource Restricted Access; Hardcopy may be available in the library Format The file format, physical medium, or dimensions of the resource online Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Faculty Publications Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Creator An entity primarily responsible for making the resource Ta, Augusty; DSouza, Greta; Augustine, Vintu Title A name given to the resource Effect of Professional Development Program in Enhancing Leadership Skills of In-Service Teachers in Diverse Domains of Practice Date A point or period of time associated with an event in the lifecycle of the resource 01-01-2025 Source A related resource from which the described resource is derived Leadership and Policy in Schools; Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1080/15700763.2025.2497375" target="_blank" rel="noreferrer noopener">https://doi.org/10.1080/15700763.2025.2497375</a> <a href="https://www.scopus.com/pages/publications/105003869337?origin=resultslist" target="_blank" rel="noreferrer noopener">https://www.scopus.com/pages/publications/105003869337?origin=resultslist</a> Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Ta A., Department of Education, CHRIST University, Bangalore, India; DSouza G., Department of Education, CHRIST University, Bangalore, India; Augustine V., Department of Education, CHRIST University, Bangalore, India Description An account of the resource In alignment with the recent National Education Policy and National Professional Standards for Teachers in India, which promote the Continuous Professional Development of Teachers (CPD), the present study developed, implemented, and evaluated a Teacher Professional Development Program on Leadership (TPDP-L) for developing and enhancing teacher leadership skills in six domains of practice. The participants (n = 54) of the study (20 from government schools, 18 from aided schools, and 16 from unaided schools) were selected through purposive sampling, ensuring diverse representation. The study employed a quasi-experimental, single-group pretest-posttest design, utilizing the Teacher Leadership Scale, a self-assessment questionnaire, to assess the programs impact. The result shows a large effect size and statistically significant differences in all leadership domains. The studys promising results suggest that TPDP-L is an evidence-based CPD program for developing and enhancing leadership skills among in-service schoolteachers. The studys findings evidence practical implications for implementing educational policies. 2025 Taylor & Francis Group, LLC. Publisher An entity responsible for making the resource available Routledge Relation A related resource ISSN: 15700763; Language A language of the resource English Type The nature or genre of the resource Article Rights Information about rights held in and over the resource Restricted Access; Hardcopy may be available in the library Format The file format, physical medium, or dimensions of the resource online Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Faculty Publications Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Creator An entity primarily responsible for making the resource TA, Augusty; DSouza, Greta; Augustine, Vintu Title A name given to the resource Effect of Professional Development Programme on Mentorship in Enhancing Self-efficacy and Outcome Expectancy of In-Service Teachers Date A point or period of time associated with an event in the lifecycle of the resource 01-01-2025 Source A related resource from which the described resource is derived International Journal of Educational Reform; Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1177/10567879251323882" target="_blank" rel="noreferrer noopener">https://doi.org/10.1177/10567879251323882</a> <a href="https://www.scopus.com/pages/publications/105000506663?origin=resultslist" target="_blank" rel="noreferrer noopener">https://www.scopus.com/pages/publications/105000506663?origin=resultslist</a> Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant TA A., School of Education, CHRIST (Deemed to be University), KA, Bangalore, India; DSouza G., School of Education, CHRIST (Deemed to be University), KA, Bangalore, India; Augustine V., School of Education, CHRIST (Deemed to be University), KA, Bangalore, India Description An account of the resource Emphasizing the importance of Continuous Professional Development programmes for teachers to ensure quality performance, Educational Policies, frameworks, and professional standards for teachers across nations around the world advocate qualitative and quantitative mentorship training for them, given the dearth of such opportunities. Holistic professional development programs for in-service teachers enhancing their mentorship skills and supporting their overall well-being have become inevitable part of the academic calendars of progressive institutions given the renewed and well-justified emphasis by policies and for their known and established benefits. Though scanty in number, integrated programs supporting the development of mentorship skills among in-service teachers have been reported to be of qualitative benefit in raising their performance bar. The present study reports the formulation and validation of a Professional Development Programme on Mentorship for in-service teachers and its implementation through an intervention adopting the quasi-experimental, single-group pre-test and post-test design. The program module, designed as per the ADDIE model, consisted of five units focusing on self-efficacy, outcome expectancy and skills development in four areas: personal, professional, instructional, and assessment. A group of 48 (n = 48) in-service teachers participated in the study and responded to the Mentor Efficacy Scale, a self-assessment questionnaire, before and after the intervention. Analysis of the pre-test and post-test data shows a significant increase in self-efficacy and outcome expectancy variables of mentorship among in-service teachers. The study's findings offer valuable insights for advocating the professional development program on mentorship skills to build and sustain a professional learning culture, a robust support system for colleagues and a positive school culture. Given the positive and promising results of the program, there is scope for further research exploring the long-term effects of the intervention with a mixed-method design. The Author(s) 2025. Subject The topic of the resource mentorship skills; outcome expectancy; Professional development; self-efficacy; teacher training Publisher An entity responsible for making the resource available SAGE Publications Inc. Relation A related resource ISSN: 10567879; Language A language of the resource English Type The nature or genre of the resource Article Rights Information about rights held in and over the resource Restricted Access; Hardcopy may be available in the library Format The file format, physical medium, or dimensions of the resource online Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Conference Papers Conference Paper Faculty Publications- Conference Papers Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Nano ZnO@PEG catalyzed one-pot green synthesis of pyrano[2,3-d] pyrimidines in ethanol via one-pot multicomponent approach Subject The topic of the resource Multicomponent reaction; Nano ZnO@PEG; Pyrano[2,3-d]pyrimidines; Three-component synthesis Description An account of the resource A facile one-pot multicomponent protocol for the synthesis of bio-active Pyrano[2,3-d]pyrimidine derivatives by a one- step condensation reaction of substituted aldehyde, malononitrile/methyl cyanoacetate, barbituric acid has been demonstrated using nano ZnO@PEG as a catalyst at room temperature. The present approach offers several advantages, such as shorter reaction time, higher yields, and environmental friendliness. Easy isolation of products, absence of column chromatographic purification, use of commercially available low-cost starting materials and reusability of the catalyst make the methodology viable in organic synthesis. 2020 Elsevier Ltd. All rights reserved. Selection and peer-review under responsibility of the scientific committee of the Second International Symposium ''Functional Nanomaterials in Industrial Applications: Academy - Industry Meet''. Creator An entity primarily responsible for making the resource Tabassum S.; Devi K.R.S.; Govindaraju S. Source A related resource from which the described resource is derived Materials Today: Proceedings, Vol-45, pp. 3716-3721. Publisher An entity responsible for making the resource available Elsevier Ltd Date A point or period of time associated with an event in the lifecycle of the resource 2020-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1016/j.matpr.2020.12.677" target="_blank" rel="noreferrer noopener">https://doi.org/10.1016/j.matpr.2020.12.677</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85107427146&doi=10.1016%2Fj.matpr.2020.12.677&partnerID=40&md5=df086ed1f6203c1fe44ee646985ba5e7" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85107427146&doi=10.1016%2fj.matpr.2020.12.677&partnerID=40&md5=df086ed1f6203c1fe44ee646985ba5e7</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 22147853 Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Conference paper Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College, South End Road, Basavanagudi, Bengaluru, 560004, India; Devi K.R.S., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, 560029, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to be University), Kumbalagodu, Mysore Road, Bengaluru, 560074, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Articles Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Yttrium(III) oxide catalyzed facile synthesis of novel hydrazinyl thiazoles by multicomponent approach Subject The topic of the resource Hydrazinyl thiazole; Multicomponent reaction; Phenacyl bromide; Three-component synthesis; Yttrium(III) oxide Description An account of the resource A facile and a one-pot procedure for the synthesis of novel hydrazinyl thiazoles by the cyclo condensation reaction between substituted phenacyl bromides, aromatic aldehydes, and semicarbazides using Yttrium(III) oxide as reusable catalyst under acetic acid as a solvent medium is described. The chromatography-free methodology has several benefits such as being facile, atom economic, higher functional group tolerance and provides excellent yield in shorter reaction time. All the synthesized compounds were characterized by 1H NMR, 13C NMR, and HRMS (ESI) analysis. 2021 Creator An entity primarily responsible for making the resource Tabassum S.; Govindaraju S. Source A related resource from which the described resource is derived Materials Today: Proceedings, Vol-54, pp. 748-752. Publisher An entity responsible for making the resource available Elsevier Ltd Date A point or period of time associated with an event in the lifecycle of the resource 2022-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1016/j.matpr.2021.11.069" target="_blank" rel="noreferrer noopener">https://doi.org/10.1016/j.matpr.2021.11.069</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85127866585&doi=10.1016%2Fj.matpr.2021.11.069&partnerID=40&md5=03163479041f0cd78864de4b40723227" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85127866585&doi=10.1016%2fj.matpr.2021.11.069&partnerID=40&md5=03163479041f0cd78864de4b40723227</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 22147853 Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Article Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College, South End Road, Basavanagudi, Bengaluru, 560004, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to be University), Kumbalagodu, Mysore Road, Bengaluru, 560074, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Articles Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource White LED Light-Mediated Eosin Y-Photocatalyzed One-Pot Synthesis of Novel 1,2,4-Triazol-3-Amines By Sequential Addition Subject The topic of the resource 1,2,4-Triazol-3-amine; Eosin Y; Four-component synthesis; Metal-free; Multicomponent reaction; Photocatalyst; White LED Description An account of the resource Abstract: A facile and proficient, eco-friendly multicomponent synthesis of 12 novel biologically essential 1,2,4-triazol-3-amines via the sequential addition of substituted phenacyl bromide, aromatic aldehyde, hydrazinecarbothioamide, and urea under white LED with eosin Y as a photocatalyst has been developed. The intrinsic advantages are methodology is cost-effective, non-toxic, generates a high yield of product, is column chromatography free and does not need the use of a specific instrument. Surprisingly, our methodology uses moderate conditions and can count the tolerance of a wide variety of electron-donating and electron-withdrawing groups. The analysis and early conclusions give more value and context for the future development of organic synthesis using photocatalysts. Graphical Abstract: [Figure not available: see fulltext.] 2022, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature. Creator An entity primarily responsible for making the resource Tabassum S.; Govindaraju S. Source A related resource from which the described resource is derived Topics in Catalysis Publisher An entity responsible for making the resource available Springer Date A point or period of time associated with an event in the lifecycle of the resource 2022-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1007/s11244-022-01590-w" target="_blank" rel="noreferrer noopener">https://doi.org/10.1007/s11244-022-01590-w</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85124333009&doi=10.1007%2Fs11244-022-01590-w&partnerID=40&md5=52804da20c24f7e81536369d2f984041" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85124333009&doi=10.1007%2fs11244-022-01590-w&partnerID=40&md5=52804da20c24f7e81536369d2f984041</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 10225528 Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Article Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College, South End Road, Basavanagudi, Bengaluru, 560004, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to be University), Kumbalagodu, Mysore Road, Bengaluru, 560074, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Articles Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource (Mes-Acr-Me)+ClO4 Catalyzed Visible Light-Supported, One-Pot Green Synthesis of 1,8-Naphthyridine-3-Carbonitriles Subject The topic of the resource 1,8-Naphthyridines; 9-Mesityl-10-methylacridinium perchlorate; Blue LED; Excellent yield; Multicomponent reaction Description An account of the resource Abstract: A novel, four-component one-pot green synthesis of biologically active 1,8-naphthyridines by a reaction of diverse aromatic aldehyde, malononitrile, 4-hydroxy substituted 1,6-dimethylpyridin-2(1H)-one, corresponding aniline in EtOH catalyzed by 9-Mesityl-10-methylacridinium perchlorate [(Mes-Acr-Me)+ClO4] under visible light generated from a 24W Blue LED wavelength 450460nm at 26C is reported. In contrast with the reported procedure, our methodology is diverse, versatile and has several favourable factors such as metal-free, excellent yields, shorter reaction durations, chromatography free and straightforward extraction process. Graphical Abstract: [Figure not available: see fulltext.]. 2022, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature. Creator An entity primarily responsible for making the resource Tabassum S.; Govindaraju S.; Kendrekar P. Source A related resource from which the described resource is derived Topics in Catalysis Publisher An entity responsible for making the resource available Springer Date A point or period of time associated with an event in the lifecycle of the resource 2022-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1007/s11244-022-01583-9" target="_blank" rel="noreferrer noopener">https://doi.org/10.1007/s11244-022-01583-9</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85124739905&doi=10.1007%2Fs11244-022-01583-9&partnerID=40&md5=5cc5bcf5db27657099ce3f95e39dfced" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85124739905&doi=10.1007%2fs11244-022-01583-9&partnerID=40&md5=5cc5bcf5db27657099ce3f95e39dfced</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 10225528 Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Article Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College, South End Road, Basavanagudi, Bengaluru, 560004, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to be University), Kumbalagodu, Mysore Road, Bengaluru, 560074, India; Kendrekar P., Lipid Nanostructures Laboratory, Centre for Smart Materials, School of Natural Sciences, University of Central Lancashire, Preston, PR1 2HE, United Kingdom Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Articles Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource One-pot sustainable synthesis of novel pyrido[2,3-d]pyrimidinones and their evaluation for antitubercular and anticancer activity Subject The topic of the resource Anticancer activity; Antitubercular activity; MCR; Pyrido[2,3-d]pyrimidinones; Sustainable synthesis; ?-proline Description An account of the resource A novel green protocol for the construction of diversified pyrido[2,3-d]pyrimidinones was accomplished by a single-pot reaction of aryl aldehydes, Meldrum's acid, thiobarbituric acid, and ammonium acetate/aniline in H2O using ?-proline as an expeditious reusable catalyst at room temperature (26 C). Our strategy provides an innovative synthetic avenue for the construction of pyrido[2,3-d]pyrimidinones, as well as several advantages over traditional methods, including a simple procedure, shorter reaction duration, excellent yields, safe handling, easy workup, catalyst recovery, and environmental compatibility. Furthermore, the synthesised compounds were tested for their impact on different cell lines and microorganisms. Compounds 5d and 5e were particularly effective against Mycobacterium tuberculosis (antitubercular), human breast cancer cells (MCF-7), lung cancer cells (A549 and NCI-H460), and both Gram-positive (S. pyogenes) and Gram-negative (E. coli) bacteria. The derivatives with hydroxyl and nitro substitutions [5e, 5f] showed the highest potency against MCF-7, A549, and NCI-H460 cell lines, with IC50 values of 3.684.36, 3.823.41, and 11.3412.28 g/mL, respectively. 2024 The Author(s) Creator An entity primarily responsible for making the resource Tabassum S.; Ramaraj S.G.; Rajprasad J.; Sadaiyandi V.; Kumar N.; Govindaraju S. Source A related resource from which the described resource is derived Journal of Organometallic Chemistry, Vol-1025 Publisher An entity responsible for making the resource available Elsevier B.V. Date A point or period of time associated with an event in the lifecycle of the resource 2025-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1016/j.jorganchem.2024.123450" target="_blank" rel="noreferrer noopener">https://doi.org/10.1016/j.jorganchem.2024.123450</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85210404206&doi=10.1016%2Fj.jorganchem.2024.123450&partnerID=40&md5=0f5d132eb2b7b9d8aa6a0284ed9acf14" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85210404206&doi=10.1016%2fj.jorganchem.2024.123450&partnerID=40&md5=0f5d132eb2b7b9d8aa6a0284ed9acf14</a> Rights Information about rights held in and over the resource All Open Access; Hybrid Gold Open Access Relation A related resource ISSN: 0022328X; CODEN: JORCA Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Article Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College - Autonomous, South End Road, Basavanagudi, Bengaluru, 560004, India; Ramaraj S.G., Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Japan, Department of Materials Physics, Saveetha School of Engineering, Saveetha Institute of Medical and Technical Sciences (SIMTS), Thandalam, Tamilnadu, Chennai, 602105, India; Rajprasad J., Department of Civil Engineering, College of Engineering and Technology, SRM Institute of Science and Technology, Kattankulathur, 603203, India; Sadaiyandi V., Department of Physics and Nanotechnology, SRM Institute of Science and Technology, Kattankulathur, Tamilnadu, Chengalpattu, 603203, India; Kumar N., Department of Electronics & Communication Engineering, Graphic Era Deemed to be University, Uttarakhand, Dehradun, 248002, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, Christ University, Mysore Road, Bengaluru, 560074, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Conference Papers Conference Paper Faculty Publications- Conference Papers Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Synthesis of 1, 8-Naphthyridine-3-Carbonitriles under solvent-free conditions using ceric ammonium nitrate Subject The topic of the resource Green chemistry; Heterocycles; Knoevenagel condensation; Michael addition; Multicomponent reaction; Solvent-free synthesis Description An account of the resource 1,8-naphthyridines are synthesized using a four-component, one-pot approach. This method includes the reaction of aromatic aldehyde, malononitrile, 1,6-dimethylpyridin-2(1H)-one, substituted aniline in a solvent-free condition catalyzed by Ceric Ammonium Nitrate (CAN). Contrary to the reported literature, this distinct method houses several promising factors to the same degree as solvent-free reaction conditions, shorter reaction duration, excellent yields, and a straightforward extraction process. 2023 Elsevier Ltd. All rights reserved. Creator An entity primarily responsible for making the resource Tabassum S.; Servesh A.; Daniel N.K.; Govindaraju S. Source A related resource from which the described resource is derived Materials Today: Proceedings, Vol-100, pp. 218-222. Publisher An entity responsible for making the resource available Elsevier Ltd Date A point or period of time associated with an event in the lifecycle of the resource 2023-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1016/j.matpr.2023.07.144" target="_blank" rel="noreferrer noopener">https://doi.org/10.1016/j.matpr.2023.07.144</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85214191018&doi=10.1016%2Fj.matpr.2023.07.144&partnerID=40&md5=c6c52499e048c28fe0309ee9f67d52af" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85214191018&doi=10.1016%2fj.matpr.2023.07.144&partnerID=40&md5=c6c52499e048c28fe0309ee9f67d52af</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 22147853 Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Conference paper Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College, Bengaluru, 560004, India; Servesh A., Department of Chemistry, CHRIST- Deemed to be University, Bengaluru, 570029, India; Daniel N.K., Department of Sciences and Humanities, CHRIST- Deemed to be University, Bengaluru, 570029, India; Govindaraju S., Department of Sciences and Humanities, CHRIST- Deemed to be University, Bengaluru, 570029, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Conference Papers Conference Paper Faculty Publications- Conference Papers Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource An insight into the superior performance of ZnO@PEG nanocatalyst for the synthesis of 1,4-dihydropyrano[2,3-c]pyrazoles under ultrasound Subject The topic of the resource 3-c]pyrazol-6-amine Four-component synthesis Multicomponent reaction; 4-dihydropyrano[2; ZnO@PEG nanoparticle Ultrasonic irradiation 1 Description An account of the resource The investigation presents a straightforward synthesis of fifteen 1,4-dihydropyrano[2,3-c]pyrazoles using ZnO@PEG nanocatalyst in ethanol via Multicomponent approach under the influence of ultrasound. The present methodology successively tolerates a variety of functional groups and offers several advantages such as excellent yields without chromatographic purification, milder reaction conditions, shorter reaction times, and the use of an environmentally benign reusable catalyst. Ecstatically, the reaction was successfully scaled to gram level ascertaining the wider applicability of ZnO@PEG nanoparticles in multicomponent reactions. 2019 Elsevier Ltd. All rights reserved. Creator An entity primarily responsible for making the resource Tabassum S.; Sunaja Devi K.R.; Govindaraju S. Source A related resource from which the described resource is derived Materials Today: Proceedings, Vol-45, pp. 3898-3903. Publisher An entity responsible for making the resource available Elsevier Ltd Date A point or period of time associated with an event in the lifecycle of the resource 2019-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1016/j.matpr.2020.06.283" target="_blank" rel="noreferrer noopener">https://doi.org/10.1016/j.matpr.2020.06.283</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85107381679&doi=10.1016%2Fj.matpr.2020.06.283&partnerID=40&md5=4c1db366d70a8877f4b75cb5cc1979cd" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85107381679&doi=10.1016%2fj.matpr.2020.06.283&partnerID=40&md5=4c1db366d70a8877f4b75cb5cc1979cd</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 22147853 Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Conference paper Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College, South End Road, Basavanagudi, Bengaluru, 560004, India; Sunaja Devi K.R., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, 560029, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to be University), Kumbalagodu, Mysore Road, Bengaluru, 560074, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Articles Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Pyrazole Derivative Containing Naphthalene Moiety: Cytotoxocity (Breast and Cervical Cancer), Antibacterial and Antifungal Studies Using Experimental and Theoretical Tools Subject The topic of the resource ADME; antibacterial; antifungal; cytotoxicity; FMO; NCI Description An account of the resource In the present study, the title compound is named 4-((5-hydroxy-3-methyl-1-phenyl-1H-pyrazol-4-yl)(6-methoxynaphthalen-1-yl)methyl)-5-methyl-2-phenyl-1,2-dihydropyrazol-3-one was synthesized, and its antibacterial, antifungal, cytotoxic activity was studied by both experimental and in silico methods. The molecular structure was optimized using DFT/B3LYP method with cc-pVDZ as a besis set, and frontier molecular orbital (FMO) studies was used to explain the physiochemical properties of that molecule by the energy of interacting orbitals. NBO describes the intra delocalization of electrons in the molecule, which support the stability of that molecule. Noncovalent interaction (NCI) explains the nonbond interactions present in the molecule. Drug-likeness property of 405 C have been checked by absorption, distribution, metabolism and excretion (ADME) assay, result shown all the drug-likeness properties in red color region, so we have confirmed this molecule as a drug. 405 C undergoes antibiotic activity against P. aeruginosa organism, antifungal activity against B. cinerea and cytotoxicity activity against MCF-7 and HeLa cell when compared to standard drugs. 2022 Taylor & Francis Group, LLC. Creator An entity primarily responsible for making the resource Tabassum S.; Thangaiyan P.; Govindaraju S.; Daniel N.K.; Thomas R. Source A related resource from which the described resource is derived Polycyclic Aromatic Compounds, Vol-43, No. 9, pp. 8544-8561. Publisher An entity responsible for making the resource available Taylor and Francis Ltd. Date A point or period of time associated with an event in the lifecycle of the resource 2023-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1080/10406638.2022.2149564" target="_blank" rel="noreferrer noopener">https://doi.org/10.1080/10406638.2022.2149564</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85143203230&doi=10.1080%2F10406638.2022.2149564&partnerID=40&md5=bcfae84144cc0c3e3f3f2940cfad5586" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85143203230&doi=10.1080%2f10406638.2022.2149564&partnerID=40&md5=bcfae84144cc0c3e3f3f2940cfad5586</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 10406638 Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Article Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College, Bengaluru, India; Thangaiyan P., Department of Chemistry, St Berchmans College, Changanaserry, India, Department of Mechanical Engineering, University Centre for Research & Development Chandigarh University, Mohali, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to Be University), Bengaluru, India; Daniel N.K., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to Be University), Bengaluru, India; Thomas R., Department of Chemistry, St Berchmans College, Changanaserry, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Faculty Publications Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Creator An entity primarily responsible for making the resource Tabassum, Sumaiya; Basha, A. Aathif; Govindaraju, Santhosh; Kubaib, Attar Title A name given to the resource Green synthesis, characterization, and therapeutic potential of 2-(Thiophen-2-ylmethylene)malononitrile: Insights into molecular interactions with cyclooxygenase-2 (COX-2) Date A point or period of time associated with an event in the lifecycle of the resource 01-01-2025 Source A related resource from which the described resource is derived Journal of Molecular Structure;Volume;1346;Issue;;Article No.;143186; Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1016/j.molstruc.2025.143186" target="_blank" rel="noreferrer noopener">https://doi.org/10.1016/j.molstruc.2025.143186</a> <a href="https://www.scopus.com/pages/publications/105009891188?origin=resultslist" target="_blank" rel="noreferrer noopener">https://www.scopus.com/pages/publications/105009891188?origin=resultslist</a> Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College - Autonomous, South End Road, Karnataka, Bengaluru, 560004, India; Basha A.A., Department of Physics, Islamiah College (Autonomous), Tamilnadu, Vaniyambadi, 635752, India, Department of Physics, KNS Institute of Technology, Karnataka, Bangalore, 560 064, India; Govindaraju S., Department of Sciences and Humanities, Christ University, Mysore Road, Karnataka, Bengaluru, 560074, India; Kubaib A., Department of Chemistry, Islamiah College (Autonomous), Tamilnadu, Vaniyambadi, 635752, India Description An account of the resource A novel bioactive molecule, 2-(thiophen-2-ylmethylene)malononitrile, was synthesized via a green chemistry approach using thiophene-2-carbaldehyde and malononitrile under sonication in ethanol. The compound was characterized by UV-visible, H NMR, C NMR, HR-MS spectroscopy, and single-crystal XRD techniques, confirming its structural integrity. Computational studies revealed its chemical reactivity, including molecular electrostatic potential (MEP), Mulliken charges, and frontier molecular orbitals (FMO). At the same time, time-dependent DFT (TD-DFT) highlighted key electronic transitions across diverse solvents. Advanced analyses, such as Hirshfeld surface mapping and electron localization functions, identified critical intermolecular interactions involving H?N, N?H, and C?H contacts. Molecular docking with Cyclooxygenase-2 (COX-2, PDB ID: 6 2j) revealed strong binding affinity, further supported by molecular dynamics simulations demonstrating complex stability through RMSD, Rg, SASA, and hydrogen bond evaluations. The compound's anti-inflammatory potential was validated in vivo using a carrageenan-induced paw oedema model in rats, showing comparable efficacy to standard drugs. This study highlights the sustainable synthesis and therapeutic promise of 2-(thiophen-2-ylmethylene)malononitrile for pharmaceutical applications. 2025 Elsevier B.V. Subject The topic of the resource Cyclooxygenase-2; In vitro study; Molecular dynamics simulation; Spectroscopic characterization; Topological and Hirshfeld surface analysis Publisher An entity responsible for making the resource available Elsevier B.V. Relation A related resource ISSN: 222860; CODEN: JMOSB Language A language of the resource English Type The nature or genre of the resource Article Rights Information about rights held in and over the resource Restricted Access; Hardcopy may be available in the library Format The file format, physical medium, or dimensions of the resource online Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Faculty Publications Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Creator An entity primarily responsible for making the resource Tabassum, Sumaiya; Govindaraju, Santhosh Title A name given to the resource White LED Light-Mediated Eosin Y-Photocatalyzed One-Pot Synthesis of Novel 1,2,4-Triazol-3-Amines By Sequential Addition Date A point or period of time associated with an event in the lifecycle of the resource 01-01-2025 Source A related resource from which the described resource is derived Topics in Catalysis;Volume;68;Issue;13;pp.1523-1533 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1007/s11244-022-01590-w" target="_blank" rel="noreferrer noopener">https://doi.org/10.1007/s11244-022-01590-w</a> <a href="https://www.scopus.com/pages/publications/85124333009?origin=resultslist" target="_blank" rel="noreferrer noopener">https://www.scopus.com/pages/publications/85124333009?origin=resultslist</a> Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College, South End Road, Basavanagudi, Bengaluru, 560004, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to be University), Kumbalagodu, Mysore Road, Bengaluru, 560074, India Description An account of the resource Abstract: A facile and proficient, eco-friendly multicomponent synthesis of 12 novel biologically essential 1,2,4-triazol-3-amines via the sequential addition of substituted phenacyl bromide, aromatic aldehyde, hydrazinecarbothioamide, and urea under white LED with eosin Y as a photocatalyst has been developed. The intrinsic advantages are methodology is cost-effective, non-toxic, generates a high yield of product, is column chromatography free and does not need the use of a specific instrument. Surprisingly, our methodology uses moderate conditions and can count the tolerance of a wide variety of electron-donating and electron-withdrawing groups. The analysis and early conclusions give more value and context for the future development of organic synthesis using photocatalysts. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022. Subject The topic of the resource 1,2,4-Triazol-3-amine; Eosin Y; Four-component synthesis; Metal-free; Multicomponent reaction; Photocatalyst; White LED Publisher An entity responsible for making the resource available Springer Relation A related resource ISSN: 10225528; Language A language of the resource English Type The nature or genre of the resource Article Rights Information about rights held in and over the resource Restricted Access; Hardcopy may be available in the library Format The file format, physical medium, or dimensions of the resource online Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Faculty Publications Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Creator An entity primarily responsible for making the resource Tabassum, Sumaiya; Govindaraju, Santhosh; Kendrekar, Pravin Title A name given to the resource (Mes-Acr-Me)+ClO4 Catalyzed Visible Light-Supported, One-Pot Green Synthesis of 1,8-Naphthyridine-3-Carbonitriles Date A point or period of time associated with an event in the lifecycle of the resource 01-01-2025 Source A related resource from which the described resource is derived Topics in Catalysis;Volume;68;Issue;13;pp.1440-1448 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1007/s11244-022-01583-9" target="_blank" rel="noreferrer noopener">https://doi.org/10.1007/s11244-022-01583-9</a> <a href="https://www.scopus.com/pages/publications/85124739905?origin=resultslist" target="_blank" rel="noreferrer noopener">https://www.scopus.com/pages/publications/85124739905?origin=resultslist</a> Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College, South End Road, Basavanagudi, Bengaluru, 560004, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, CHRIST (Deemed to be University), Kumbalagodu, Mysore Road, Bengaluru, 560074, India; Kendrekar P., Lipid Nanostructures Laboratory, Centre for Smart Materials, School of Natural Sciences, University of Central Lancashire, Preston, PR1 2HE, United Kingdom Description An account of the resource Abstract: A novel, four-component one-pot green synthesis of biologically active 1,8-naphthyridines by a reaction of diverse aromatic aldehyde, malononitrile, 4-hydroxy substituted 1,6-dimethylpyridin-2(1H)-one, corresponding aniline in EtOH catalyzed by 9-Mesityl-10-methylacridinium perchlorate [(Mes-Acr-Me)+ClO4] under visible light generated from a 24W Blue LED wavelength 450460nm at 26C is reported. In contrast with the reported procedure, our methodology is diverse, versatile and has several favourable factors such as metal-free, excellent yields, shorter reaction durations, chromatography free and straightforward extraction process. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022. Subject The topic of the resource 1,8-Naphthyridines; 9-Mesityl-10-methylacridinium perchlorate; Blue LED; Excellent yield; Multicomponent reaction Publisher An entity responsible for making the resource available Springer Relation A related resource ISSN: 10225528; Language A language of the resource English Type The nature or genre of the resource Article Rights Information about rights held in and over the resource Restricted Access; Hardcopy may be available in the library Format The file format, physical medium, or dimensions of the resource online Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Faculty Publications Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Creator An entity primarily responsible for making the resource Tabassum, Sumaiya; Ramaraj, Sankar Ganesh; Rajprasad, J.; Sadaiyandi, Vivekananthan; Kumar, Niraj; Govindaraju, Santhosh Title A name given to the resource One-pot sustainable synthesis of novel pyrido[2,3-d]pyrimidinones and their evaluation for antitubercular and anticancer activity Date A point or period of time associated with an event in the lifecycle of the resource 01-01-2025 Source A related resource from which the described resource is derived Journal of Organometallic Chemistry;Volume;1025;Issue;;Article No.;123450; Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1016/j.jorganchem.2024.123450" target="_blank" rel="noreferrer noopener">https://doi.org/10.1016/j.jorganchem.2024.123450</a> <a href="https://www.scopus.com/pages/publications/85210404206?origin=resultslist" target="_blank" rel="noreferrer noopener">https://www.scopus.com/pages/publications/85210404206?origin=resultslist</a> Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tabassum S., Department of Chemistry, Surana College - Autonomous, South End Road, Basavanagudi, Bengaluru, 560004, India; Ramaraj S.G., Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, 7-3-1 Hongo, Japan, Department of Materials Physics, Saveetha School of Engineering, Saveetha Institute of Medical and Technical Sciences (SIMTS), Thandalam, Tamilnadu, Chennai, 602105, India; Rajprasad J., Department of Civil Engineering, College of Engineering and Technology, SRM Institute of Science and Technology, Kattankulathur, 603203, India; Sadaiyandi V., Department of Physics and Nanotechnology, SRM Institute of Science and Technology, Kattankulathur, Tamilnadu, Chengalpattu, 603203, India; Kumar N., Department of Electronics & Communication Engineering, Graphic Era Deemed to be University, Uttarakhand, Dehradun, 248002, India; Govindaraju S., Department of Sciences and Humanities, School of Engineering and Technology, Christ University, Mysore Road, Bengaluru, 560074, India Description An account of the resource A novel green protocol for the construction of diversified pyrido[2,3-d]pyrimidinones was accomplished by a single-pot reaction of aryl aldehydes, Meldrum's acid, thiobarbituric acid, and ammonium acetate/aniline in H2O using ?-proline as an expeditious reusable catalyst at room temperature (26 C). Our strategy provides an innovative synthetic avenue for the construction of pyrido[2,3-d]pyrimidinones, as well as several advantages over traditional methods, including a simple procedure, shorter reaction duration, excellent yields, safe handling, easy workup, catalyst recovery, and environmental compatibility. Furthermore, the synthesised compounds were tested for their impact on different cell lines and microorganisms. Compounds 5d and 5e were particularly effective against Mycobacterium tuberculosis (antitubercular), human breast cancer cells (MCF-7), lung cancer cells (A549 and NCI-H460), and both Gram-positive (S. pyogenes) and Gram-negative (E. coli) bacteria. The derivatives with hydroxyl and nitro substitutions [5e, 5f] showed the highest potency against MCF-7, A549, and NCI-H460 cell lines, with IC50 values of 3.684.36, 3.823.41, and 11.3412.28 g/mL, respectively. 2024 The Author(s) Subject The topic of the resource Anticancer activity; Antitubercular activity; MCR; Pyrido[2,3-d]pyrimidinones; Sustainable synthesis; ?-proline Publisher An entity responsible for making the resource available Elsevier B.V. Relation A related resource ISSN: 0022328X; CODEN: JORCA Language A language of the resource English Type The nature or genre of the resource Article Rights Information about rights held in and over the resource All Open Access; Hybrid Gold Open Access Format The file format, physical medium, or dimensions of the resource online Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Faculty Publications Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Creator An entity primarily responsible for making the resource Tadepalli, Srinivas; Rathore, Mahendra Singh; Ballal, Suhas; Thangavelu, Indumathi; Gadallah, Abdelrahman G. Title A name given to the resource Biogenic Carboxymethyl Cellulose and L-Histidine Coated Barium Peroxide Nanocomposite: A Tri-Functional Platform Targeting Antimicrobial Resistance, Cancer, and Oxidative Stress Date A point or period of time associated with an event in the lifecycle of the resource 01-01-2026 Source A related resource from which the described resource is derived Polymers for Advanced Technologies;Volume;37;Issue;1;Article No.;e70508; Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1002/pat.70508" target="_blank" rel="noreferrer noopener">https://doi.org/10.1002/pat.70508</a> <a href="https://www.scopus.com/pages/publications/105028264937?origin=resultslist" target="_blank" rel="noreferrer noopener">https://www.scopus.com/pages/publications/105028264937?origin=resultslist</a> Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tadepalli S., Department of Chemical Engineering, College of Engineering, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, Saudi Arabia; Rathore M.S., Department of Applied Science, PIT, Parul University, Gujarat, Vadodara, India; Ballal S., Department of Biochemistry, School of Sciences, JAIN (Deemed-to-be University), Karnataka, India; Thangavelu I., Department of Chemistry, CHRIST (Deemed to be University), Bangalore, India; Gadallah A.G., Department of Chemical Engineering, College of Engineering, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, Saudi Arabia Description An account of the resource The study addresses the urgent need for novel therapeutic agents in combating multidrug-resistant pathogens, cancer, and oxidative stress-related diseases. Barium peroxide (BaO2) nanoparticles and its novel nanocomposite, carboxymethyl cellulose and L-histidine coated BaO2 (BaO2-CMC-LH) were synthesized, characterized, and evaluated for their antibacterial, anticancer, and DPPH radical scavenging activities. Structural and functional characterizations were carried out using various analytical techniques. Biological evaluations demonstrated enhanced antibacterial activity against Methicillin-resistant Staphylococcus aureus (MRSA) and Candida albicans (C. albicans), with BaO2-CMC-LH exhibiting superior inhibition zones compared to BaO2. For MRSA, the zone of inhibition (ZOI) for BaO2 is about 9 mm, whereas the BaO2-CMC-LH nanocomposite exhibits a substantially larger ZOI of 21 mm. Likewise, for C. albicans, BaO2 presents a ZOI of 12 mm, and BaO2-CMC-LH exhibits a greater inhibition zone of 18 mm. Cytotoxicity analysis against osteosarcoma MG-63 cells revealed significantly improved anticancer activity, with BaO2-CMC-LH achieving an IC?? value of 28.6 ?g/mL compared to 53.3 ?g/mL for BaO2. The 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay showed that the BaO2-CMC-LH nanocomposite (78.45%) had activity compared to BaO2 alone (64.43%). These findings underscore the synergistic effects of the CMC-LH matrix in enhancing BaO2's biological activities, positioning BaO2-CMC-LH as a promising multifunctional therapeutic agent for addressing global health challenges. 2026 John Wiley & Sons Ltd. Subject The topic of the resource barium peroxide; Candida albicans; carboxymethyl cellulose; DPPH free radical scavenging assay; L-histidine; MRSA; osteosarcoma MG-63 Publisher An entity responsible for making the resource available John Wiley and Sons Ltd Relation A related resource ISSN: 10427147; Language A language of the resource English Type The nature or genre of the resource Article Rights Information about rights held in and over the resource All Open Access; Bronze Open Access Format The file format, physical medium, or dimensions of the resource online Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Reviews Review Faculty Publications- Reviews Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource A review on synthetic approaches towards kavalactones Subject The topic of the resource 5,6-dihydropyrones; Biological activity; Chiral auxiliary; Lactones; Lipase resolution; Natural products; Total synthesis; ?-pyrones Description An account of the resource Kavalactones are classes of ?-pyrone and 5,6-dihydropyrone derivatives showing various biological activities, and numerous approaches have been reported for the preparation of these molecules. In this review, we discuss the different synthetic approaches towards these naturally occurring lactones, in both racemic and enantiomerically pure forms, that have been reported in the literature to date. It is hoped that this review will assist researchers in the development of additional and efficient synthetic routes towards kavalactones. 1 Introduction 2 Synthetic Approaches for the Preparation of Kavalactones 3 Conclusion. 2021. Thieme. Creator An entity primarily responsible for making the resource Tadiparthi K.; Anand P. Source A related resource from which the described resource is derived Synthesis (Germany), Vol-53, No. 19, pp. 3469-3484. Publisher An entity responsible for making the resource available Georg Thieme Verlag Date A point or period of time associated with an event in the lifecycle of the resource 2021-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1055/s-0040-1706044" target="_blank" rel="noreferrer noopener">https://doi.org/10.1055/s-0040-1706044</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85106938214&doi=10.1055%2Fs-0040-1706044&partnerID=40&md5=a39b797d04bfa1a0ab1675c38bb553bc" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85106938214&doi=10.1055%2fs-0040-1706044&partnerID=40&md5=a39b797d04bfa1a0ab1675c38bb553bc</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 397881; CODEN: SYNTB Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Review Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tadiparthi K., Department of Chemistry, CHRIST (Deemed to Be University), Hosur Road, Bangalore, 560026, India; Anand P., Department of Chemistry, CHRIST (Deemed to Be University), Hosur Road, Bangalore, 560026, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Reviews Review Faculty Publications- Reviews Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource A Journey toward the Syntheses of ?-Amino-?-hydroxybutyric Acid (GABOB) and Carnitine Subject The topic of the resource ascorbic acid; carnitine; GABOB; lipase resolution; mannitol; Sharpless dihydroxylation; total synthesis Description An account of the resource In this review, we discuss the synthetic approaches to ?-amino-?-hydroxybutyric acid (GABOB) and carnitine from 1980 to date. The unique structure and biological importance of these molecules have created much interest in various synthetic approaches over the last four decades by organic chemists from across the world. Most of the syntheses are asymmetric methods that involved chiral pool, enantioselective synthesis, enzyme resolution, or a chiral auxiliary as a source of chirality, and the biological significance of the molecules was also discussed. The compiled synthetic methods may fill the existence gap, simplify the complexity involved in the synthesis, and allow the best synthetic route to be found by comparison of all the methods. However, this review also will be useful to prepare similar kind of scaffolds present in various complex natural products. 2021 American Chemical Society Creator An entity primarily responsible for making the resource Tadiparthi K.; Anand P. Source A related resource from which the described resource is derived Organic Process Research and Development, Vol-25, No. 9, pp. 2008-2019. Publisher An entity responsible for making the resource available American Chemical Society Date A point or period of time associated with an event in the lifecycle of the resource 2021-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1021/acs.oprd.1c00027" target="_blank" rel="noreferrer noopener">https://doi.org/10.1021/acs.oprd.1c00027</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85114356150&doi=10.1021%2Facs.oprd.1c00027&partnerID=40&md5=53cf592d9b72348c9acb064d976c35ee" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85114356150&doi=10.1021%2facs.oprd.1c00027&partnerID=40&md5=53cf592d9b72348c9acb064d976c35ee</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 10836160; CODEN: OPRDF Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Review Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tadiparthi K., Department of Chemistry, CHRIST (Deemed to be University), Hosur Road, Bangalore, 560026, India; Anand P., Department of Chemistry, CHRIST (Deemed to be University), Hosur Road, Bangalore, 560026, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Articles Article Faculty Publications -Articles Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Desymmetrisation of meso-2,4-Dimethyl-8-oxabicyclo[3.2.1]-oct-6-ene-3-ol and its Application in Natural Product Syntheses Subject The topic of the resource Chiral pool; Dimethyl-8-oxa-bicyclo[3.2.1]oct-6-en-3-ol; Hydroboration; Lactone; Natural products; Total synthesis Description An account of the resource The compounds containing chiral centers and different functional groups serve as magnificent building blocks for the preparation of various natural products that are having immense biological activity. Dimethyl-8-oxa-bicyclo[3.2.1]oct-6-en-3-ol is one of the wonderful synthons to construct multiple stereo centers at a time during the asymmetric synthesis. In this account, we discuss our research efforts toward the synthesis of various simple and complex natural products from the past three decades (19952020) by using dimethyl-8-oxa-bicyclo[3.2.1]oct-6-en-3-ol as a synthon. Moreover, the synthetic utility of this starting material was investigated and well demonstrated. Further, we executed the desymmetrization of dimethyl-8-oxa-bicyclo[3.2.1]oct-6-en-3-ol by hydroboration to get different chiral centers. After obtaining the stereocenters, we could manage either the fragment, formal or total synthesis of natural products, by simple protection and deprotection sequence followed by C?C bond formation steps. 2021 The Chemical Society of Japan & Wiley-VCH GmbH Creator An entity primarily responsible for making the resource Tadiparthi K.; Anand P.; Sakirolla R.; Gupta T.P.; Jadhav K.A.; Kishore Das S.; Singh Yadav J. Source A related resource from which the described resource is derived Chemical Record, Vol-22, No. 3 Publisher An entity responsible for making the resource available John Wiley and Sons Inc Date A point or period of time associated with an event in the lifecycle of the resource 2022-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1002/tcr.202100286" target="_blank" rel="noreferrer noopener">https://doi.org/10.1002/tcr.202100286</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85121334577&doi=10.1002%2Ftcr.202100286&partnerID=40&md5=6841fc6870588d1ce2ad042b10fcfc14" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85121334577&doi=10.1002%2ftcr.202100286&partnerID=40&md5=6841fc6870588d1ce2ad042b10fcfc14</a> Rights Information about rights held in and over the resource Restricted Access Relation A related resource ISSN: 15278999; PubMed ID: 34894063; CODEN: CRHEA Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Article Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tadiparthi K., Department of Chemistry, CHRIST (Deemed to be University), Hosur Road, Bangalore, 560029, India, Natural Product Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad, 500007, India; Anand P., Department of Chemistry, CHRIST (Deemed to be University), Hosur Road, Bangalore, 560029, India; Sakirolla R., Department of Chemistry, Central University of Karnataka, Gulbarga, Karnataka, 585367, India, Natural Product Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad, 500007, India; Gupta T.P., School of Science, Indrashil University, Kadi, Mehsana, Gujarat, 382740, India; Jadhav K.A., School of Science, Indrashil University, Kadi, Mehsana, Gujarat, 382740, India; Kishore Das S., School of Science, Indrashil University, Kadi, Mehsana, Gujarat, 382740, India; Singh Yadav J., Natural Product Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad, 500007, India, School of Science, Indrashil University, Kadi, Mehsana, Gujarat, 382740, India Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Reviews Review Faculty Publications- Reviews Dublin Core The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/. Title A name given to the resource Synthetic Approaches to Diospongins: A Two Decade Journey Subject The topic of the resource asymmetric allylation; cross-metathesis; diarylheptanoids; diospongins; enzyme resolution; hetero-Diels-Alder reaction; oxa-Michael addition; Prins cyclization; tetrahydropyran Description An account of the resource Tetrahydropyran units having multiple stereogenic centers serve as excellent building blocks for various active pharmaceutical ingredients (APIs). In particular, the presence of the unique molecular architecture of the trisubstituted tetrahydropyran (THP) unit in diospongins enhances their biological activity due to multiple stereogenic centers and has attracted attention from the synthetic community over the last two decades. In this review, we discuss synthetic approaches to chiral and racemic forms of diospongins during the period 2006 2020 in chronological order. 2022 by the authors. Creator An entity primarily responsible for making the resource Tadiparthi K.; Chatterjee S. Source A related resource from which the described resource is derived SynOpen, Vol-6, No. 3, pp. 141-157. Publisher An entity responsible for making the resource available Georg Thieme Verlag Date A point or period of time associated with an event in the lifecycle of the resource 2022-01-01 Identifier An unambiguous reference to the resource within a given context <a href="https://doi.org/10.1055/s-0040-1720032" target="_blank" rel="noreferrer noopener">https://doi.org/10.1055/s-0040-1720032</a> <a href="https://www.scopus.com/inward/record.uri?eid=2-s2.0-85134516337&doi=10.1055%2Fs-0040-1720032&partnerID=40&md5=584b745ab72135479cc6cdd0ccbb89a6" target="_blank" rel="noreferrer noopener">https://www.scopus.com/inward/record.uri?eid=2-s2.0-85134516337&doi=10.1055%2fs-0040-1720032&partnerID=40&md5=584b745ab72135479cc6cdd0ccbb89a6</a> Rights Information about rights held in and over the resource All Open Access; Gold Open Access Relation A related resource ISSN: 25099396 Format The file format, physical medium, or dimensions of the resource Online Language A language of the resource English Type The nature or genre of the resource Review Coverage The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant Tadiparthi K., Department of Chemistry, CHRIST (Deemed to Be University), Hosur Road, Bangalore, 560029, India; Chatterjee S., Department of Chemistry, CHRIST (Deemed to Be University), Hosur Road, Bangalore, 560029, India