期刊
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 17, 期 -, 页码 800-804出版社
BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.17.68
关键词
acylation; kinetic resolution; nucleophilic catalysis; paracyclophanes; planar chirality
资金
- Austrian Science Funds (FWF) [P31784]
- European Union through the EFRE INTERREG IV ETC-AT-CZ program [M00146]
- Austrian Science Fund (FWF) [P31784] Funding Source: Austrian Science Fund (FWF)
This study presents a method for the kinetic resolution of racemic 4-hydroxy[2.2]paracyclophane through a chiral isothiourea-catalyzed acylation reaction, which allows for a synthetically useful s-factor of 20 and provides a novel entry to obtain this interesting planar chiral motive in an enantioenriched manner.
We herein report a method for the kinetic resolution of racemic 4-hydroxy[2.2]paracyclophane by means of a chiral isothiourea-catalyzed acylation with isobutyric anhydride. This protocol allows for a reasonable synthetically useful s-factor of 20 and provides a novel entry to obtain this interesting planar chiral motive in an enantioenriched manner.
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