Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/71447
標題: New beta-amino thiols as efficient catalysts for highly enantioselective alkenylzinc addition to aldehydes
作者: Tseng, S.L.
Yang, T.K.
關鍵字: asymmetric-synthesis;organozinc reagents;carbonyl-compounds;grignard-reagents;alcohols;diethylzinc;zinc;disulfide
Project: Tetrahedron-Asymmetry
期刊/報告no:: Tetrahedron-Asymmetry, Volume 16, Issue 4, Page(s) 773-782.
摘要: 
A series of new optically active beta-amino thiols and thiolacetates prepared from the simple natural amino acid, (S)-(-)-valine, were found to be effective catalysts for the enantioselective addition of alkenylzinc to alclehydes and thereby providing an efficient route for chiral (E)-allylic alcohols with ees of up to >99% in the presence of 7a (1 mol %). (C) 2005 Published by Elsevier Ltd.
URI: http://hdl.handle.net/11455/71447
ISSN: 0957-4166
DOI: 10.1016/j.tetasy.2004.11.093
Appears in Collections:期刊論文

Show full item record
 

Google ScholarTM

Check

Altmetric

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.