Molecular Iodine Mediated Domino Reaction for Synthesis of Benzamides, 2,2-diazidobenzofuran-3(2H)-ones and Benzoxazolones

Rajendar, K; Kant, Ruchir; Narender, T

dc.contributor.author	Rajendar, K
dc.contributor.author	Kant, Ruchir
dc.contributor.author	Narender, T
dc.date.accessioned	2014-07-31T10:11:02Z
dc.date.available	2014-07-31T10:11:02Z
dc.date.issued	2013
dc.identifier.citation	Advanced Synthesis & Catalysis, 2013, 355(18), 3591–3596	en
dc.identifier.uri	http://hdl.handle.net/123456789/1325
dc.description.abstract	A simple and efficient domino protocol has been developed for the preparation of biologically important benzamides, 2,2-diazidobenzofuran-3(2H)-ones and benzoxazolones from various structurally and electronically divergent acetophenones and o-hydroxy acetophenones in the presence of molecular iodine, sodium azide and sodium bicarbonate at 100 °C in good to excellent yields.	en
dc.format.extent	192949 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CSIR-CDRI Communication No. 8574	en
dc.subject	Benzoxazolone	en
dc.subject	Benzamide	en
dc.subject	2,2-Diazidobenzofuran-3(2H)-One	en
dc.subject	Iodine	en
dc.subject	Sodium Azide	en
dc.subject	Curtius Rearrangement	en
dc.subject	Haller-Bauer Reaction	en
dc.title	Molecular Iodine Mediated Domino Reaction for Synthesis of Benzamides, 2,2-diazidobenzofuran-3(2H)-ones and Benzoxazolones	en
dc.type	Article	en