4.8 Article

Catalytic enantioselective synthesis of quaternary all-carbon stereogenic centers.: Preparation of α,α'-disubstituted β,γ-unsaturated esters through Cu-catalyzed asymmetric allylic alkylations

Journal

ORGANIC LETTERS
Volume 7, Issue 7, Pages 1255-1258

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol047331r

Keywords

-

Funding

  1. NIGMS NIH HHS [GM-47480] Funding Source: Medline

Ask authors/readers for more resources

Peptide-based chiral ligands, readily prepared from commercially available materials, are used to promote Cu-catalyzed asymmetric allylic alkylations of alpha,beta-unsaturated esters bearing a gamma-phosphate with various alkylzinc reagents. These transformations lead to the formation of alpha,alpha'-dialkyl-beta,gamma-unsaturated esters in high yields as well as high regio- (re) and enantioselectivities (ee).

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