期刊
ORGANIC LETTERS
卷 19, 期 15, 页码 4126-4129出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b01936
关键词
-
资金
- National Natural Science Foundation of China [21602023, 21672158]
- Chongqing Research and Frontier Technology [cstc2016jcyjA0403]
- National University of Singapore [R-143-000-599-112]
A phosphine-catalyzed highly enantioselective [4 + 2] annulation between ortho-quinone methides and allene ketones has been developed. The reported method led to the formation of chromane derivatives in high yields and excellent enantioselectivity. This is the first time that ortho-quinone methides are employed in phosphine-mediated cyclization reactions.
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