Synthesis of 6H-Isoindolo[2,1-a]indol-6-ones through Wittig reaction and tandem reductive cyclization-lactamization

Kadam, H.K.; Tilve, S.G.

dc.contributor.author	Kadam, H.K.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2015-06-04T03:40:32Z
dc.date.available	2015-06-04T03:40:32Z
dc.date.issued	2013
dc.identifier.citation	European Journal of Organic Chemistry. 2013(20); 2013; 4280-4284.	en_US
dc.identifier.uri	http://dx.doi.org/10.1002/ejoc.201300047
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/2874
dc.description.abstract	A convenient and efficient two-step route to 6H-Isoindolo[2,1-a]indol-6-ones has been developed starting from o-nitrobenzaldehydes. The methodology involves Wittig reaction followed by tandem reductive cyclization-lactamization. A series of isoindoloindolones incorporating different substituents on the indole nucleus has been prepared.	en_US
dc.publisher	Wiley-VCH Verlag	en_US
dc.subject	Chemistry	en_US
dc.title	Synthesis of 6H-Isoindolo[2,1-a]indol-6-ones through Wittig reaction and tandem reductive cyclization-lactamization	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y