Journal
ORGANIC LETTERS
Volume 13, Issue 16, Pages 4272-4275Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol201620g
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [20972157]
- 973 Program [2009CB825300]
- Natural Science Foundation of Liaoning Province [20102225]
- CAS [DICP K2009D04]
Ask authors/readers for more resources
An efficient palladium(0)-catalyzed, Cu(I)-mediated synthetic route to trisubstituted olefins and conjugate dienes has been developed via oxo directing Liebeskind-Srogl cross-coupling reactions of gem-dihaloolefin-type alpha-oxo ketene dithioacetals with aryl and alkenylboronic acids. The synthetic protocol has demonstrated rare examples of transition-metal-promoted transformations of ketene dithioacetals, providing a novel route to highly functionalized conjugate dienes.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available