Access to di- and tri-Substituted Oxazoles via an NBS-Mediated Oxidative Cyclisation of N-acylaminoacid Derivatives†

Bathula, S R; Reddy, M P; Viswanadham, K K D R; Sathyanarayana, Pochampalli; Reddy, M S

dc.contributor.author	Bathula, S R
dc.contributor.author	Reddy, M P
dc.contributor.author	Viswanadham, K K D R
dc.contributor.author	Sathyanarayana, Pochampalli
dc.contributor.author	Reddy, M S
dc.date.accessioned	2013-10-04T09:35:46Z
dc.date.available	2013-10-04T09:35:46Z
dc.date.issued	2013
dc.identifier.citation	European Journal of Organic Chemistry, 2013, 2013(21), 4552–4557	en
dc.identifier.uri	http://hdl.handle.net/123456789/1131
dc.description.abstract	A remarkably simple method for the synthesis of various di- and tri-substituted functionalized oxazoles is described in metal or any catalyst free conditions. An iterative bromination and debromination of N-acylated aminoacid derivatives using NBS as the sole reagent cleanly led to various substituted oxazoles.	en
dc.format.extent	262983 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CDRI Communication No. 8474	en
dc.subject	Acyl amino acids	en
dc.subject	N-Bromosuccinamide	en
dc.subject	Bromination	en
dc.subject	Oxidative cyclisation	en
dc.subject	Oxazoles	en
dc.title	Access to di- and tri-Substituted Oxazoles via an NBS-Mediated Oxidative Cyclisation of N-acylaminoacid Derivatives†	en
dc.type	Article	en