Formal acylamination of nitroalkenes in aqueous medium for the synthesis of 2-aryl-3-nitro-2,3-dihydro-quinolin-4(1H)-ones

Chaturvedi, A K; Rastogi, Namrata

dc.contributor.author	Chaturvedi, A K
dc.contributor.author	Rastogi, Namrata
dc.date.accessioned	2017-05-30T07:42:53Z
dc.date.available	2017-05-30T07:42:53Z
dc.date.issued	2015
dc.identifier.citation	Synthesis 2015, 47, 249–255	en
dc.identifier.uri	http://hdl.handle.net/123456789/1693
dc.description.abstract	Formal acylamination of aromatic nitroalkenes with 2-aminobenzoyl benzotriazoles in aqueous methanol results into diastereoselective synthesis of 2-aryl-3-nitro-2,3-dihydro-quinolin-4(1H)-ones. The aliphatic nitroalkenes however form Michael addition product with benzotriazole	en
dc.format.extent	223665 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CSIR-CDRI Communication No. is 8762	en
dc.subject	Acylamination	en
dc.subject	Nitroalkenes	en
dc.subject	N-(2-aminobenzoyl)benzotriazole	en
dc.subject	2-aryl-3-nitro-2,3-dihydroquinolin-4(1H)-one	en
dc.subject	Diastereoselective	en
dc.title	Formal acylamination of nitroalkenes in aqueous medium for the synthesis of 2-aryl-3-nitro-2,3-dihydro-quinolin-4(1H)-ones	en
dc.type	Article	en