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Copper-catalyzed cascade reactions of substituted 4-iodo-pyrazolecarbaldehydes with 1,2-phenylenediamines and 2-aminophenols

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

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Field Value
 
Creator Nayak, Maloy
Batra, Sanjay
 
Date 2011-03-17T05:30:06Z
2011-03-17T05:30:06Z
2010
 
Identifier Adv. Synth. Catal. 2010, 352, 3431 – 3437
http://hdl.handle.net/123456789/649
 
Description A new approach for the synthesis of novel annulated-pyrazoles is presented. This protocol includes an intermolecular condensation followed by a copper-mediated intramolecular C-N or C-O coupling reaction. The method is applied to a range of substituted 4-iodopyrazolecarbaldehydes which react with 1,2-phenylenediamines or 2-aminophenols to yield substituted-2,4 or 1,4-dihydrobenzo[b]pyrazolo[4,3-e][1,4]diazepines or substituted-2H or 1H-benzo[b]pyrazolo[3,4-f][1,4]oxazepines, respectively.
 
Format 183556 bytes
application/pdf
 
Language en
 
Relation CDRI Communication No 7986
 
Subject Pyrazole
Copper
C-N coupling
C-O coupling
diazepines
oxazepines
 
Title Copper-catalyzed cascade reactions of substituted 4-iodo-pyrazolecarbaldehydes with 1,2-phenylenediamines and 2-aminophenols
 
Type Article