Journal
ORGANIC LETTERS
Volume 7, Issue 17, Pages 3821-3824Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol051533l
Keywords
-
Categories
Ask authors/readers for more resources
A general route to enantioenriched tert-butyl 3,3-diarylpropanoates is presented. These useful building blocks are prepared via an asymmetric rhodium-catalyzed conjugate addition of arylboronic acids to unsaturated tert-butyl esters in the presence of chiral dienes as ligands. The addition of both electron-poor and electron-rich boronic acids proceeds smoothly with various enoates in 63-90% yield with high enantioselectivites (89-94% ee).
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