Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5289634 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
A method for the enantioselective synthesis of homopropargylic alcohols using indium under Barbier-like conditions is reported herein. Both aromatic and aliphatic aldehydes were successfully converted to the corresponding homopropargylic alcohols in good yield and high enantiomeric excesses using propargyl bromide, indium, and (1S,2R)-(+)-2-amino-1,2-diphenylethanol as a chiral auxiliary.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lacie C. Hirayama, Kevin K. Dunham, Bakthan Singaram,