期刊
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
卷 95, 期 8, 页码 1217-1219出版社
CHEMICAL SOC JAPAN
DOI: 10.1246/bcsj.20220096
关键词
Asymmetric acylation; meso-1,2-Diol; Chiral 1,2-diamine
资金
- Japan Society for the Promotion of Science KAKENHI [JP21K05065]
The one-pot desymmetrization of meso-1,2-diols was successfully achieved via benzoylation and subsequent silylation, leading to the formation of corresponding siloxy esters with excellent enantioselectivities. The reduction of these siloxy esters produced the corresponding beta-siloxy alcohols without any loss in enantioselectivity.
The one-pot desymmetrization of meso-1,2-diols was successfully performed via their benzoylation, and subsequent silylation to give the corresponding siloxy esters in excellent enantioselectivities. The reduction of these siloxy esters afforded the corresponding beta-siloxy alcohols without any loss in enantioselectivity.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据