Iodine-mediated electrophilic tandem cyclization of 2-alkynylbenzaldehydes with anthranilic acid leading to 1,2-dihydroisoquinoline-fused benzoxazinones§

Dighe, S U; Batra, Sanjay

dc.contributor.author	Dighe, S U
dc.contributor.author	Batra, Sanjay
dc.date.accessioned	2014-06-23T09:12:40Z
dc.date.available	2014-06-23T09:12:40Z
dc.date.issued	2013
dc.identifier.citation	Tetrahedron, 2013, 69(46), 9875–9885	en
dc.identifier.uri	http://hdl.handle.net/123456789/1292
dc.description.abstract	An efficient iodine-mediated electrophilic tandem cyclization of substituted 2-alkynylbenzaldehydes with anthranilic acids under basic medium leading to iodo-1,2-dihydroisoquinoline-fused benzoxazinones is presented. Success of the protocol for the reaction of substituted 2-alkynylbenzaldehydes with 2- aminobenzamides to furnish isoquinoline-fused quinazolinones is also described.	en
dc.format.extent	366503 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CSIR-CDRI Communication No. 8525	en
dc.subject	Iodine	en
dc.subject	Heterocycle	en
dc.subject	Tandem	en
dc.subject	Anthranilic acid	en
dc.subject	Isoquinoline	en
dc.title	Iodine-mediated electrophilic tandem cyclization of 2-alkynylbenzaldehydes with anthranilic acid leading to 1,2-dihydroisoquinoline-fused benzoxazinones§	en
dc.type	Article	en