期刊
ORGANIC LETTERS
卷 21, 期 18, 页码 7645-7648出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b02952
关键词
-
资金
- Alexander von Humboldt Foundation for the Research Group Linkage Programme
- (Albert-Ludwigs-Universitat Freiburg)
The silver(I)-catalyzed reaction of ortho-alkynylbenzaldoximes with propargylic alcohols represents a new strategy for the divergent one-pot synthesis of 2-(isoquinolin-1-yl) prop-2-en-1-ones via tandem 6-endo-cyclization, 1,3-dipolar cycloaddition, and intramolecular dehydrative opening of the 2,3-dihydroisoxazole ring. This synthetic protocol tolerates a wide variety of ortho-alkynylbenzaldoximes and propargylic alcohols and affords the corresponding products in excellent yields.
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