Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/71439
標題: A facile method for the synthesis of enantiopure alpha-unsubstituted beta-hydroxy esters
作者: Wang, Y.C.
Hwang, J.Y.
Chen, Y.C.
Chuang, S.C.
Yan, T.H.
關鍵字: asymmetric aldol reaction;silyl ketene acetals;achiral aldehydes;enolate
Project: Tetrahedron-Asymmetry
期刊/報告no:: Tetrahedron-Asymmetry, Volume 11, Issue 8, Page(s) 1797-1800.
摘要: 
One-pot deacylation-debromination reactions involving the transesterification of the initial chiral beta-bromo-beta-hydroxy thioimide aldol adducts and subsequent Al-Hg mediated reductive cleavage of the C-Br bond allow for a facile synthesis of enantiopure beta-hydroxy esters. (C) 2000 Published by Elsevier Science Ltd.
URI: http://hdl.handle.net/11455/71439
ISSN: 0957-4166
DOI: 10.1016/s0957-4166(00)00109-9
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.