4.8 Article

Catalytic asymmetric Simmons-Smith cyclopropanation of silyl enol ethers. Efficient synthesis of optically active cyclopropanol derivatives

Journal

ORGANIC LETTERS
Volume 8, Issue 13, Pages 2827-2829

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol0609659

Keywords

-

Ask authors/readers for more resources

This paper describes a catalytic asymmetric Simmons-Smith cyclopropanation of silyl enol ethers using dipeptide 2 as the ligand. A variety of optically active cyclopropyl silyl ethers can be obtained in high yields. Up to 96% ee was obtained. The dipeptide can be recovered after the reaction in good yield and reused without the loss of reactivity or enantioselectivity.

Authors

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

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available