Department of Chemistry, Northeast Normal University , Changchun 130024, China.
Chem Rev. 2016 Jan 27;116(2):287-322. doi: 10.1021/acs.chemrev.5b00360. Epub 2016 Jan 13.
Push-pull alkenes, which bear electron-donating and -accepting group(s) at both termini of a C═C double bond, respectively, are of interest not only for their unique electronic properties but also for their importance as versatile building blocks in organic synthesis. In the world of ketene acetals having the push-pull alkene skeleton, ketene N,S-acetal is most likely the biggest family according to the number and types of these compounds. The first ketene N,S-acetal compound was reported in 1956. As a cyclic ketene N,S-acetal compound, nithiazine, the first lead structure of neonicotinoid insecticides, was reported in 1978. The characteristics of ketene N,S-acetals, which have the structural feature of ketene S,S-acetals and enaminones, make them versatile and easy to use, especially in cyclization and multicomponent reactions for the synthesis of various heterocyclic systems and related natural products. There has been an increasing wealth of information about the synthesis and synthetic applications of ketene N,S-acetals, especially, in recent years. This review provides comprehensive knowledge on the chemistry of ketene N,S-acetals.
推-拉烯,其在 C=C 双键的两端分别带有供电子和吸电子基团,不仅因其独特的电子性质而受到关注,而且还因其作为有机合成中多功能构建块的重要性而受到关注。在具有推-拉烯骨架的偕二酮缩醛世界中,根据这些化合物的数量和类型,偕二酮 N,S-缩醛最有可能是最大的家族。第一个偕二酮 N,S-缩醛化合物于 1956 年报道。作为环状偕二酮 N,S-缩醛化合物,噻嗪,新烟碱类杀虫剂的第一个先导结构,于 1978 年报道。偕二酮 N,S-缩醛的特点具有偕二酮 S,S-缩醛和烯胺酮的结构特征,使它们具有多功能性和易用性,特别是在环化和多组分反应中,用于合成各种杂环系统和相关的天然产物。近年来,关于偕二酮 N,S-缩醛的合成和合成应用的信息越来越丰富。这篇综述提供了关于偕二酮 N,S-缩醛化学的全面知识。