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 InfoField | 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
|
|