期刊
CHEMICAL COMMUNICATIONS
卷 48, 期 46, 页码 5796-5798出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cc31553j
关键词
-
资金
- National Natural Science Foundation of China [20902084, 21172199]
- Program for Changjiang Scholars and Innovative Research Team in Chinese Universities [IRT0980]
An unprecedented Pd-catalyzed hydrohalogenation of alkynyl halides for the regio- and stereoselective synthesis of (Z)-1,2-dihaloalkenes has been realized using [(allyl)PdCl](2) as the catalyst and cis, cis-1,5-cyclooctadiene as the ligand. The advantages of this protocol are well illustrated by the assembly of trisubstituted (Z)-enynes and multifunctional benzenes via iterative cross-coupling reactions or tandem Diels-Alder-aromatization reactions, respectively.
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