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Field Value
 
Creator Mayani, VJ
Abdi, SHR
Kureshy, RI
Khan, NUH
Das, A
Bajaj, HC
 
Subject Chemistry
 
Description Chiral amino alcohols supported on mesoporous silicas were synthesized and evaluated as a new class of chiral ligands in copper-catalyzed nitroaldol reaction under heterogeneous and mild reaction conditions. The activity and enantioselectivity of the present catalytic system is immensely influenced by the presence of achiral and chiral bases as an additive. The heterogenized chiral copper(II) complex of amino alcohol was found to be an effective recyclable catalyst for the nitroaldol reaction of different aldehydes such as aromatic, aliphatic, alicyclic, and alpha-beta unsaturated aldehydes to produce nitroaldol products with remarkably high enantioselectivity (>= 99%) and yields.
 
Publisher AMER CHEMICAL SOCWASHINGTON1155 16TH ST, NW, WASHINGTON, DC 20036 USA
 
Date 2011-09-20T12:03:11Z
2011-09-20T12:03:11Z
2010
 
Type Article
 
Identifier JOURNAL OF ORGANIC CHEMISTRY
0022-3263
http://hdl.handle.net/123456789/12208
 
Language English