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[3+3] Cycloaddition of Azomethine Imine: Synthesis of Bi- or Tricyclic N-Heterocycle

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CHEMISTRYSELECT
卷 5, 期 25, 页码 7605-7626

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.202001674

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Azomethine imine; Asymmetric Synthesis; Metal catalyzed approach; Metal free protocol; Six membered N-heterocycles; Biographical sketch

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  1. TEQIP III

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Synthesis of six-membered bicyclic, tricyclic or tetracyclic N-heterocycles are important due to enormous use of such scaffolds in bioactive natural products, agrochemicals and in pharmaceuticals. [3+3] cycloaddition of azomethine imine for the construction of such heterocycles is less explored but also a genuine approach with the other method like [4+2] and [2+2+2] cycloaddition. Hence, the literature survey in this area is utmost significant. The delights and difficulties of [3+3] cycloaddition of azomethine imine have been deliberated thoroughly to elucidate this highly mounting field in this literature study. Herein, we report a vast synthetic method [base catalyzed, metal catalyzed (racemic and asymmetric), phosphine catalyzed, NHC and Lewis acid catalyzed] for the synthesis of di, tri and tetra-nitrogen containing heterocycles via [3+3] cycloadditon reaction of azomethine imine.

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