Recent Advances in Organocatalyzed Asymmetric Sulfa-Michael Addition Triggered Cascade Reactions

Cheng Niu, Da Ming Du*

*此作品的通讯作者

科研成果: 期刊稿件文献综述同行评审

8 引用 (Scopus)

摘要

The sulfa-Michael addition reaction is a crucial subset of the Michael addition reaction, and aroused the interest of numerous synthetic biologists and chemists. In particular, sulfa-Michael addition triggered cascade reaction has developed quickly in recent years because it offers an efficient method to construct C−S bonds and other bonds in one approach, which is widely applicable for building chiral pharmaceuticals, their intermediates, and natural compounds. This review emphasizes the recent advancements in sulfa-Michael addition-triggered cascade reactions for the stereoselective synthesis of sulfur-containing compounds, including sulfa-Michael/aldol, sulfa-Michael/Henry, sulfa-Michael/Michael, sulfa-Michael/Mannich and some sulfa-Michael triggered multi-step processes. Moreover, some reaction mechanisms and derivatization experiments are introduced appropriately.

源语言英语
文章编号e202200258
期刊Chemical Record
23
7
DOI
出版状态已出版 - 7月 2023

指纹

探究 'Recent Advances in Organocatalyzed Asymmetric Sulfa-Michael Addition Triggered Cascade Reactions' 的科研主题。它们共同构成独一无二的指纹。

引用此

Niu, C., & Du, D. M. (2023). Recent Advances in Organocatalyzed Asymmetric Sulfa-Michael Addition Triggered Cascade Reactions. Chemical Record, 23(7), 文章 e202200258. https://doi.org/10.1002/tcr.202200258