期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 15, 期 22, 页码 4803-4806出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ob00762k
关键词
-
资金
- National Natural Science Foundation of China [21472042]
- Jiangsu Province Funds for Distinguished Young Scientists [BK20160005]
- Qing-Lan Project
- Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, Changzhou University
A Pd(0)/(S)-p-MeO-BnPHOX catalytic system has been established for the asymmetric reductive Heck reaction of (Z)-1-iodo-1,6-dienes, which affords quaternary tetrahydropyridines with good to excellent enantioselectivities. This reaction tolerates a wide range of substituted alkene moieties, including 1,1-disubstituted, 1,1,2-trisubstituted as well as 1,2-disubstituted alkenes.
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