Affiliation:
1. Key Laboratory of Structure-Based Drugs Design and Discovery (Ministry of Education), School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China
Abstract
Imines, versatile intermediates for organic synthesis, can be exploited for the
preparation of diverse classes of biologically active benzazoles. Because of the special
characteristics of the C=N bond, imines can be simultaneously used in the synthesis of
1,3-benzazoles and 1,2-benzazoles. With the development of imine synthesis, a variety of
novel cascade reactions for benzazole synthesis have been reported in the last decade.
Therefore, there is a strong need to elucidate the recent progress in the formation of various
classes of benzazoles, including benzimidazoles, benzoxazoles, benzothiazoles, indazoles,
and benzisoxazoles, via imines obtained by condensation reactions or oxidative/
redox coupling reactions In this review, we provide a comprehensive survey of this
area. In particular, various green and mild synthetic methodologies are summarized, and
the multiple roles of novel catalysts and significant mechanisms for several transformations are highlighted in
detail. We believe that this review will aid researchers studying the synthesis of complex molecules containing
the benzazole motif via imines.
Funder
Shenyang Pharmaceutical University
Natural Science Foundation of Liaoning Province
National Natural Science Foundation of China
Publisher
Bentham Science Publishers Ltd.
Cited by
9 articles.
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