CSIR Central

Facile Synthesis of 11-aryl-6H-isoindolo [2,1-a]indol-6-ones via Hypervalent Iodine (III)-Promoted Cascade Cyclization

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

View Archive Info
 
 
Field Value
 
Creator Dev, Kapil
Maurya, Rakesh
 
Date 2015-03-20T04:57:47Z
2015-03-20T04:57:47Z
2015
 
Identifier RSC Advances. 2015, 5, 13102-13106
http://hdl.handle.net/123456789/1429
 
Description An efficient method was developed for the synthesis of tetracyclic fused indoleandisoindoline ring system, under metal-free conditions. The hypervalent iodine PIDA-mediated regioselective as well as chemoselective intramolecular cascade oxidative cyclization of 2-(1-arylethynyl)benzamides afforded 11-aryl-6H-isoindolo [2,1-a] indol-6-ones at room temperature in good to excellent yields.
 
Format 245624 bytes
application/pdf
 
Language en
 
Relation CSIR-CDRI Communication No. 8894
 
Subject Tetracyclic
Hypervalent Iodine
 
Title Facile Synthesis of 11-aryl-6H-isoindolo [2,1-a]indol-6-ones via Hypervalent Iodine (III)-Promoted Cascade Cyclization
 
Type Article