首页 | 本学科首页   官方微博 | 高级检索  
     


Enantioselective Reactions of N‐Acyliminium Ions Using Chiral Organocatalysts
Authors:Prof. Dr. Yong Sup Lee  Md. Maqusood Alam  Dr. Rangappa S Keri
Affiliation:1. Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, 1‐Hoegi‐dong, Dongdaemoon‐ku, Seoul 130‐701 (Republic of Korea), Fax: (+82)?2‐966‐3885;2. Department of Pharmacy, College of Pharmacy, Kyung Hee University, 1‐Hoegi‐dong, Dongdaemoon‐ku, Seoul 130‐701 (Republic of Korea), Fax: (+82)?2‐966‐3885
Abstract:
N‐acyliminium ions are reactive intermediates that can act as electron‐deficient electrophiles toward weak or soft nucleophiles, thereby providing useful methods for both intermolecular‐ and intramolecular carbon–carbon and carbon–heteroatom bond formation. Nucleophilic additions to N‐acyliminium ions constitute an important method for providing α‐functionalized amino compounds and many other biologically active nitrogen‐containing heterocycles. The development of efficient catalytic asymmetric reactions is a key objective in modern organic chemistry and is very important for the synthesis of natural products, pharmaceuticals, and agrochemicals. Various methods are available for this purpose and mostly rely on the use of chiral catalysts for enantioselective synthesis. This review deals with one aspect of such catalysis, which has emerged only in the past few years, and its applications in enantioselective reactions of N‐acyliminium ions to provide various nitrogen‐containing heterocycles.
Keywords:asymmetric synthesis  heterocycles  n‐acyliminium ions  nucleophilic addition  organocatalysis
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号