Synthetic studies on biscembranoids: asymmetric total synthesis of methyl sarcoate
摘要:
The asymmetric total synthesis of a marine natural product, methyl sarcoate, has been achieved featuring the asymmetric Michael addition, the dithiane coupling, the Kosugi-Migita-Stille coupling, and the ring-closing metathesis. (C) 2005 Elsevier Ltd. All rights reserved.
Asymmetric synthesis based on chiral diamines having pyrrolidine ring
作者:Teruaki Mukaiyama
DOI:10.1016/s0040-4020(01)93286-7
日期:——
Various highly stereoselective asymmetric reactions based on chiral diamines having pyrrolidine ring are described. Some of these reactions have been successfully applied to the syntheses of natural products.