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Cascade intermolecular Michael addition-intramolecular azide/ internal alkyne 1,3-dipolar cycloaddition reaction in one-pot

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

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Field Value
 
Creator Arigela, R K
Mandadapu, A K
Sharma, S K
Kumar, Brijesh
Kundu, Bijoy
 
Date 2012-09-17T10:41:08Z
2012-09-17T10:41:08Z
2012
 
Identifier Organic Letters, 2012, 14 (7), 1804–1807
http://hdl.handle.net/123456789/918
 
Description A rapid one-pot protocol for the synthesis of indole-based polyheterocycles via a sequential Lewis acid catalyzed intermolecular Michael addition and an intramolecular azide/internal alkyne 1,3-dipolar cycloaddition reaction has been described. The generality of the method has been demonstrated by treating a series of aromatic/aliphatic 2-alkynyl indoles with substituted (E)-1-azido-2-(2-nitrovinyl)benzenes to furnish annulated tetracyclic indolo[2,3-c][1,2,3]triazolo[1,5-a][1]benzazepines in good yields.
 
Format 124693 bytes
application/pdf
 
Language en
 
Relation CDRI Communication No.8217
 
Subject Polyheterocycles
2-alkynyl
Tetracyclic indolo
1,3-dipolar cycloaddition
 
Title Cascade intermolecular Michael addition-intramolecular azide/ internal alkyne 1,3-dipolar cycloaddition reaction in one-pot
 
Type Article