当前位置:群英聚首 > 论文著作 > 正文
Enantioselective formation of quaternary carbon stereocenters in natural product synthesis: a recent update.
来源:刘国都教授个人网站 发布日期:2019-09-30
作者:Chengxi Li, Sherif Shaban Ragab, Guodu Liu,* Wenjun Tang.*
关键字:Quaternary carbon stereocenter
论文来源:期刊
具体来源:Nat. Prod. Rep., 2019, just accepted. (DOI: 10.1039/c9np00039a, review, IF = 11.876)
发表时间:2019年
Natural products bearing quaternary carbon stereocenters have attracted tremendous interest from the synthetic community due to their diverse biological activities and fascinating molecular architectures. However, the construction of these molecules in an enantioselective fashion remains a long-standing challenge because of the lack of efficient asymmetric catalytic methods for installing these motifs. The rapid progress in the development of new-generation efficient chiral catalysts has opened the door for several asymmetric reactions, such as Michael addition, dearomative cyclization, polyene cyclization, α-arylation, cycloaddition, allylation, for the construction of quaternary carbon stereocenters in a highly enantioselective fashion. These asymmetric catalytic methods have greatly facilitated the synthesis of complex natural products with improved output and overall efficiency. In this concise review, we highlight the progress in the last six years in complex natural product synthesis, in which at least one quaternary carbon stereocenter has been constructed via asymmetric catalytic technologies, with particular emphasis on the analysis of the stereochemical model of each enantioselective transformation.
Copyright © 2005 Polymer.cn All rights reserved
中国聚合物网 版权所有
经营性网站备案信息

京公网安备11010502032929号

工商备案公示信息

京ICP证050801号

京ICP备12003651号