4.7 Article

Catalytic asymmetric desymmetrization of meso-diamide derivatives through enantioselective N-allylation with a chiral π-allyl Pd catalyst:: Improvement and reversal of the enantioselectivity

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 71, Issue 6, Pages 2524-2527

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo052488y

Keywords

-

Ask authors/readers for more resources

[GRAPHICS] In the presence of the Trost ligands-Pd catalysts, N-monoallylation of bis(2,4,6-triisopropylbenzne)sulfonylamides derived from mesa-1,2-diamines proceeds with good to excellent enantioselectivity (85-96% ee) to give asymmetric desymmetrization products. Under the same conditions, in the reaction with meso-bistolunesulfonylamide derivatives, reversal of the enantioselectivity is observed.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available