跳转至内容
Merck

First diastereoselective chiral synthesis of (-)-securinine.

Organic letters (2004-01-03)
Toshio Honda, Hidenori Namiki, Kyosuke Kaneda, Hirotake Mizutani
摘要

[reaction: see text] A diastereoselective total synthesis of securinine in optically pure form was achieved by employing ring-closing metathesis of the corresponding dienyne compound as a key step.

材料
货号
品牌
产品描述

Sigma-Aldrich
3-丁烯基溴化镁 溶液, 0.5 M in THF
Sigma-Aldrich
Securinine, ≥98% (HPLC)