期刊
ISCIENCE
卷 14, 期 -, 页码 88-+出版社
CELL PRESS
DOI: 10.1016/j.isci.2019.03.010
关键词
-
资金
- Thousand Youth Talents Plan
- National Natural Science Foundation of China [21672235, 21871287]
- Strategic Priority Research Program of the Chinese Academy of Sciences [XDB20000000]
- CAS Key Laboratory of Synthetic Chemistry of Natural Substances
- Shanghai Institute of Organic Chemistry
Two catalytic asymmetric vinylogous aldol-type reactions of aldehydes with ally! phosphonate and allyl sulfone have been uncovered in good to high yields for the first time, The bulky ligand-(R)-DTBM-SEGPHOS-was found to be the key to perfectly control both regio- and enantioselectivities. Transformations of the vinylogous products (including Horner-Wadsworth-Emmons and Julia olefinations) were successfully realized by virtue of the phosphonate and sulfone moieties. Moreover, the present methodology was successfully applied in the asymmetric synthesis of natural products.
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