A convenient protocol for C-H oxidation mediated by an azido radical culminating in Ritter-type amidation

dc.contributor.author	Vijay Nair, G
dc.contributor.author	Suja, T D
dc.contributor.author	Kishor Mohanan
dc.date.accessioned	2015-09-14T17:00:14Z
dc.date.available	2015-09-14T17:00:14Z
dc.date.issued	2005
dc.identifier.citation	Tetrahedron Letters 46(18):3217-3219; 2 May 2005	en_US
dc.identifier.issn	0040-4039
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/2052
dc.description.abstract	Cerium(IV) ammonium nitrate in combination with sodium azide reacts with Unactivated hydrocarbons in acetonitrile to furnish acetamides in one pot. The strategy can be used to introduce nitrogen functionality into a variety of compounds; a carboxylic ester directly afforded the corresponding alpha-amino acid.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsevier	en_US
dc.subject	Cerium ammonium nitrate	en_US
dc.subject	CH activation	en_US
dc.subject	Ritter reaction	en_US
dc.subject	Azides	en_US
dc.subject	Radicals	en_US
dc.title	A convenient protocol for C-H oxidation mediated by an azido radical culminating in Ritter-type amidation	en_US
dc.type	Article	en_US