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                <text>Patent Number: 202221053302, Applicant: Raghvendra Omprakash Singh.&#13;
IoT and deep learning based Emotion and hate speech recognition to examine the person mind state in home/health care ABSTRACT There are several applications for AEE, which stands for automatic emotion recognition. Various industries, including advertising, technology, and human-robot interactions, use the emotional responses of individuals as a signal. This paper analyses all pertinent scientific literature to determine the application of sensors. In these publications, numerous strategies that have already been researched or implemented are discussed.</text>
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                <text>Study On Impact of Employee Retention Strategies on Employee Turnover in IT IndustryAn Exploratory Study in Bangalore



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                <text>Employee  Turnover  is  a  major  challenge  faced  by  the  companies  globally.  Employee Turnover is predominant not only in IT sector, but in other sectors as well. This study has focused in IT sector. Employees are the assets of any organization. Organizations are striving to  retain  their  talents  by  implementing   effective  retention  strategies.  High  Employee Turnover would subsequently have an impact on productivity and sustainability of the organization.



There are two types of Employee Turnover ?? functional and dysfunctional. When productive employees leave the organization, it is said to be dysfunctional turnover and when the poor performers leave, it is called functional turnover. The focus of this study was dysfunctional turnover. Dysfunctional turnover is the concern of HR managers.



When an employee leaves, it takes approximately eight weeks for this position to be replaced and  in  the  meantime,  productivity  suffers.  Causes  and  consequences  of  the  Employee Turnover is mentioned in detail in Chapter 2.



This  study  is  an  attempt  to  understand  the  impact  of  Retention  Strategies  on  Employee Turnover  in IT sector in India. Bangalore,  being the IT hub of India, was chosen  as the location of the study. Results of the study showed that Retention Strategies has an impact on Employee Turnover. Other variables such as Welfare Benefits, Personal Satisfaction and Organization Culture, which are said to be associated with the Employee Turnover were also investigated as a part of this study.

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                <text>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</text>
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                <text>White LED Light-Mediated Eosin Y-Photocatalyzed One-Pot Synthesis of Novel 1,2,4-Triazol-3-Amines By Sequential Addition</text>
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                <text>1,2,4-Triazol-3-amine; Eosin Y; Four-component synthesis; Metal-free; Multicomponent reaction; Photocatalyst; White LED</text>
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                <text>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.</text>
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                <text>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</text>
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                <text>(Mes-Acr-Me)+ClO4 Catalyzed Visible Light-Supported, One-Pot Green Synthesis of 1,8-Naphthyridine-3-Carbonitriles</text>
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              <elementText elementTextId="112969">
                <text>1,8-Naphthyridines; 9-Mesityl-10-methylacridinium perchlorate; Blue LED; Excellent yield; Multicomponent reaction</text>
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                <text>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.</text>
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                <text>Tabassum S.; Govindaraju S.; Kendrekar P.</text>
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              <elementText elementTextId="112976">
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                <text>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</text>
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                <text>One-pot sustainable synthesis of novel pyrido[2,3-d]pyrimidinones and their evaluation for antitubercular and anticancer activity</text>
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                <text>Anticancer activity; Antitubercular activity; MCR; Pyrido[2,3-d]pyrimidinones; Sustainable synthesis; ?-proline</text>
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                <text>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)</text>
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                <text>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 &amp;amp; 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</text>
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                <text>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.</text>
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                <text>Materials Today: Proceedings, Vol-100, pp. 218-222.</text>
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                <text>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</text>
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                <text>An insight into the superior performance of ZnO@PEG nanocatalyst for the synthesis of 1,4-dihydropyrano[2,3-c]pyrazoles under ultrasound</text>
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              <elementText elementTextId="187015">
                <text>3-c]pyrazol-6-amine Four-component synthesis Multicomponent reaction; 4-dihydropyrano[2; ZnO@PEG nanoparticle Ultrasonic irradiation 1</text>
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                <text>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.</text>
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                <text>Tabassum S.; Sunaja Devi K.R.; Govindaraju S.</text>
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                <text>Materials Today: Proceedings, Vol-45, pp. 3898-3903.</text>
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                <text>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</text>
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                <text>Pyrazole Derivative Containing Naphthalene Moiety: Cytotoxocity (Breast and Cervical Cancer), Antibacterial and Antifungal Studies Using Experimental and Theoretical Tools</text>
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              <elementText elementTextId="102484">
                <text>ADME; antibacterial; antifungal; cytotoxicity; FMO; NCI</text>
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                <text>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 &amp;amp; Francis Group, LLC.</text>
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                <text>Tabassum S.; Thangaiyan P.; Govindaraju S.; Daniel N.K.; Thomas R.</text>
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                <text>Polycyclic Aromatic Compounds, Vol-43, No. 9, pp. 8544-8561.</text>
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              <elementText elementTextId="102488">
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                <text>&lt;a href="https://doi.org/10.1080/10406638.2022.2149564" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1080/10406638.2022.2149564&lt;/a&gt;
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                <text>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 &amp;amp; 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</text>
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                <text>A review on synthetic approaches towards kavalactones</text>
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                <text>5,6-dihydropyrones; Biological activity; Chiral auxiliary; Lactones; Lipase resolution; Natural products; Total synthesis; ?-pyrones</text>
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                <text>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.</text>
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                <text>Synthesis (Germany), Vol-53, No. 19, pp. 3469-3484.</text>
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                <text>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</text>
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                <text>A Journey toward the Syntheses of ?-Amino-?-hydroxybutyric Acid (GABOB) and Carnitine</text>
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                <text>ascorbic acid; carnitine; GABOB; lipase resolution; mannitol; Sharpless dihydroxylation; total synthesis</text>
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                <text>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</text>
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                <text>Organic Process Research and Development, Vol-25, No. 9, pp. 2008-2019.</text>
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                <text>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</text>
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