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Field Value
 
Creator Khan, NUH
Saravanan, S
Kureshy, RI
Abdi, SHR
Sadhukhan, A
Bajaj, HC
 
Subject Chemistry
 
Description Chiral dimeric vanadium (V) salen complex (10 mol%) derived from 5,5-Methylene di-[(S,S)-{N-(3-tert-butyl salicylidine)-N'-(3',5'-di-tert-butyl salicylidene)]-1,2-cyclohexanediamine] with vanadyl suphate followed by auto oxidation was used as efficient catalyst for enantioselective Strecker reaction of N-benzylimines with TMSCN at -30 degrees C. Excellent yield (92%) of alpha-aminonitrile and high chiral induction was achieved (ee up to 94%) in case of 2-methoxy substituted N-benzylimines in 10 h. The catalytic system worked well up to four cycles with retention of enantioselectivity. (C) 2010 Published by Elsevier B. V.
 
Publisher ELSEVIER SCIENCE SALAUSANNEPO BOX 564, 1001 LAUSANNE, SWITZERLAND
 
Date 2011-09-20T12:03:18Z
2011-09-20T12:03:18Z
2010
 
Type Article
 
Identifier JOURNAL OF ORGANOMETALLIC CHEMISTRY
0022-328X
http://hdl.handle.net/123456789/12270
 
Language English