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Interesting results of catalytic hydrogenation of 3-(2-nitrophenyl)-isoxazoles and 3-(nitro-substituted-phenyl)-2-isoxazolines

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

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Field Value
 
Creator Singh, Vijay
Madapa, Sudharshan
Yadav, G P
Maulik, P R
Batra, Sanjay
 
Date 2007-12-25T10:25:20Z
2007-12-25T10:25:20Z
2006
 
Identifier Syntheis, (2006), 1995-2004
http://hdl.handle.net/123456789/42
 
Description The Pd-C-assisted hydrogenolysis of substituted 3-(2-nitrophenyl)-isoxazoles, irrespective of substitution on the isoxa-zole ring, invariably leads to reduction of nitro to amino group with concomitant regiospecific ring closure to yield substituted 4-quinolinamines. In contrast similar hydrogenation of 3-(nitro substituted phenyl)-2-isoxazolines results in reduction of the nitro group only with conservation of isoxazoline ring to yield 3-(amino substituted phenyl)-2-isoxazolines.
 
Format 253839 bytes
application/pdf
 
Language en
 
Relation CDRI Communication no 6402
 
Subject Isoxazole
2-isoxazoline
4-aminoquinoline
hydrogenation
Pd-C
ring transformation
regiospecific
 
Title Interesting results of catalytic hydrogenation of 3-(2-nitrophenyl)-isoxazoles and 3-(nitro-substituted-phenyl)-2-isoxazolines
 
Type Article