Journal
TETRAHEDRON LETTERS
Volume 44, Issue 32, Pages 6161-6163Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(03)01392-3
Keywords
trifluoromethylated amino alcohol; chiral ligand; enantioselective Reformatsky reaction
Categories
Ask authors/readers for more resources
The enantioselective Reformatsky reaction of PhCHO was achieved by the use of trifluoromethylated amino alcohols as chiral ligands to afford the corresponding optically active beta-hydroxy ester with up to 90% ee. (C) 2003 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
Recommended
No Data Available
Share Paper
