Domino Bischler-Napieralski - Michael reaction and oxidation, a new route to Coumarin-Pyrrole-Isoquinoline fused pentacycles

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

dc.contributor.author	Mandrekar, K.S.
dc.contributor.author	Kadam, H.K.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2018-12-17T09:49:05Z
dc.date.available	2018-12-17T09:49:05Z
dc.date.issued	2018
dc.identifier.citation	European Journal of Organic Chemistry. 47; 2018; 6665-6670.	en_US
dc.identifier.uri	https://doi.org/10.1002/ejoc.201801244
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/5548
dc.description.abstract	Lamellarin scaffold is synthesized by a metal free convergent route involving domino Bischler-Napieralski reaction - Michael reaction - oxidation sequence. Six lamellarin analogues were synthesised having substituent on aryl as well as coumarin ring A.	en_US
dc.publisher	Wiley-VCH	en_US
dc.subject	Chemistry	en_US
dc.title	Domino Bischler-Napieralski - Michael reaction and oxidation, a new route to Coumarin-Pyrrole-Isoquinoline fused pentacycles	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y