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              <text>Aza-Michael addition of 1,2-diazoles to structurally diverse enones: Efficient methods toward ?-amino ketones</text>
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              <text>1,2-diazoles; aza-Michael addition; cyclic enones; N-cycloalkyl heterocycles; T3P-mediated</text>
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              <text>An efficient and mild protocol was realized using 1,2-diazoles and related heterocycles with cyclic and acyclic enones in presence of T3P (2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxide) toward the regioselective formation of N-cycloalkyl heterocycles at room temperature. The developed reaction conditions showcased good selectivity over a wide range of 1,2-diazoles and enones by delivering N-cycloalkyl heterocycles in excellent yields.  2020 Wiley Periodicals LLC.</text>
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              <text>Polina S.; Putta V.P.R.K.; Gujjarappa R.; Pujar P.P.; Malakar C.C.</text>
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              <text>Journal of Heterocyclic Chemistry, Vol-58, No. 4, pp. 1029-1033.</text>
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              <text>2021-01-01</text>
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              <text>&lt;a href="https://doi.org/10.1002/jhet.4221" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1002/jhet.4221&lt;/a&gt;
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              <text>ISSN: 0022152X; CODEN: JHTCA</text>
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              <text>Polina S., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, India; Putta V.P.R.K., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, India; Gujjarappa R., Department of Chemistry, National Institute of Technology Manipur, Imphal, India; Pujar P.P., Department of Chemistry, CHRIST (Deemed to be University), Bengaluru, India; Malakar C.C., Department of Chemistry, National Institute of Technology Manipur, Imphal, India</text>
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