Effect ofMicrowave-Assisted on the N-Alkylation and N-Acylation of Cyclic Sulfamides

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DC Field	Value	Language
dc.contributor.author	Mohamed DEHAMCHIA	-
dc.contributor.author	Zine RÉGAÏNIA	-
dc.date.accessioned	2015-05	-
dc.date.available	2015-05	-
dc.date.issued	2015-05	-
dc.identifier.issn	2170-0672	-
dc.identifier.uri	http://dspace.univ-ouargla.dz/jspui/handle/123456789/9976	-
dc.description	Annales des Sciences et Technologie	en_US
dc.description.abstract	Cyclic sulfamides were efficiently N-acylated and N-alkylated with different alkyl, benzyl and acylhalides. The reactions were carried out under microwave irradiation conditions with and without solvent. A comparison with conventional methods demonstrates the advantages of applying microwave irradiation as a non-conventional method for activation in organic syntheses and chemical transformations. The structures of the synthesized compounds were inferred from their analytical and spectral data	en_US
dc.language.iso	en	en_US
dc.relation.ispartofseries	volume 7 numéro 1 AST 2015;	-
dc.subject	Microwave	en_US
dc.subject	Cyclic sulfamides	en_US
dc.subject	alkyl halide	en_US
dc.subject	acyl halide	en_US
dc.subject	N-alkylation	en_US
dc.subject	N-acylation	en_US
dc.title	Effect ofMicrowave-Assisted on the N-Alkylation and N-Acylation of Cyclic Sulfamides	en_US
dc.type	Article	en_US
Appears in Collections:	volume 7 numéro 1 AST 2015

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