An alternate route to substituted 6,7-dihydro 5H-dibenz[c,e]azepines from allylbenzamides derived from the Morita-Baylis-Hillman adducts

Bhowmik, Subhendu; Bhattacharyya, Soumya; Batra, Sanjay

dc.contributor.author	Bhowmik, Subhendu
dc.contributor.author	Bhattacharyya, Soumya
dc.contributor.author	Batra, Sanjay
dc.date.accessioned	2014-08-12T07:01:54Z
dc.date.available	2014-08-12T07:01:54Z
dc.date.issued	2014
dc.identifier.citation	Tetrahedron, 2014, 70(26), 4031–4037	en
dc.identifier.uri	http://hdl.handle.net/123456789/1364
dc.description.abstract	An acid-catalyzed modular synthesis of substituted 5H-dibenz [c,e]azepines from a biaryl allyl benzamides prepared from the MBH adducts via a cascade dearoylation and intramolecular cyclization is described. The utility of the product for preparing 7,9-dihydro-4bH-dibenz [c,e]pyrrolo[1,2-a]azepine is also presented.	en
dc.format.extent	205955 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CSIR-CDRI Communication No. 8664	en
dc.subject	Morita-Baylis-Hillman	en
dc.subject	Biaryl Allyl Benzamides	en
dc.title	An alternate route to substituted 6,7-dihydro 5H-dibenz[c,e]azepines from allylbenzamides derived from the Morita-Baylis-Hillman adducts	en
dc.type	Article	en