4.0 Article

Cu(I)-catalyzed asymmetric α-hydroxylation of β-keto esters in the presence of chiral phosphine-Schiff base-type ligands

Journal

TETRAHEDRON-ASYMMETRY
Volume 21, Issue 7, Pages 794-799

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2010.05.011

Keywords

-

Funding

  1. Shanghai Municipal Committee of Science and Technology [06XD14005, 08dj1400100-2]
  2. National Basic Research Program of China (973) [2010CB833302]
  3. National Natural Science Foundation of China [20902019, 20872162, 20672127, 20821002, 20732008, 20702059]

Ask authors/readers for more resources

Chiral phosphine-Schiff base-type ligand L1 prepared from (R)-(-)-2-(diphenylphosphino)-1,1'-binaphthyl-2'-amine was found to be a fairly effective ligand for Cu(I)-promoted enantioselective alpha-hydroxylation of beta-keto esters using oxaziridine 2a as the oxidant to give the corresponding products in high yields along with moderate enantioselectivines (C) 2010 Elsevier Ltd All rights reserved

Authors

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

Reviews

Primary Rating

4.0
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available