Oxidative coupling-type mechanism of N,N-dialkylanilines in solvent-free conditions forming crystal violet derivatives. A clay-mediated and microwave-promoted approach

dc.contributor.author	Penieres-Carrillo, G
dc.contributor.author	Ortega-Alfaro, MC
dc.contributor.author	Gutierrez-Perez, R
dc.contributor.author	Toscano, RA
dc.contributor.author	Alvarez-Toledano, C
dc.contributor.author	López-Cortes, JG
dc.date.accessioned	2011-01-22T10:27:29Z
dc.date.available	2011-01-22T10:27:29Z
dc.date.issued	2000
dc.identifier.issn	0008-4042
dc.identifier.uri	http://hdl.handle.net/11154/2034
dc.description.abstract	In the clay-mediated reaction of N,N-disubstituted anilines using microwave radiation as an energy source in the absence of solvent, crystal violet and derivatives, diphenylmethanes, and biphenyls were isolated along with intermediates supporting an oxidative coupling-type mechanism.	en_US
dc.language.iso	en	en_US
dc.title	Oxidative coupling-type mechanism of N,N-dialkylanilines in solvent-free conditions forming crystal violet derivatives. A clay-mediated and microwave-promoted approach	en_US
dc.type	Article	en_US
dc.identifier.idprometeo	2443
dc.source.novolpages	78(10):1299-1304
dc.subject.wos	Chemistry, Multidisciplinary
dc.description.index	WoS: SCI, SSCI o AHCI
dc.subject.keywords	clay
dc.subject.keywords	dyes
dc.subject.keywords	microwave radiation
dc.subject.keywords	solvent-free reactions
dc.relation.journal	Canadian Journal of Chemistry-Revue Canadienne De Chimie