dc.creatorGONZALEZ GONZALEZ, CARLOS A.;x1242037
dc.creatorMEJIA VEGA, JUAN JAVIER; 783856
dc.creatorGARCIA MONROY, RICARDO; 894517
dc.creatorGONZALEZ CALDERON, DAVIR; 277100
dc.creatorCorona Becerril, David; 122549
dc.creatorFUENTES BENITES, MARIA PAULINA AYDEE GRACIA; 21179
dc.creatorTAMARIZ MASCARUA, JOAQUIN; 1265
dc.creatorGONZALEZ ROMERO, CARLOS; 218870
dc.creatorGONZALEZ GONZALEZ, CARLOS A.
dc.creatorMEJIA VEGA, JUAN JAVIER
dc.creatorGARCIA MONROY, RICARDO
dc.creatorGONZALEZ CALDERON, DAVIR
dc.creatorCorona Becerril, David
dc.creatorFUENTES BENITES, MARIA PAULINA AYDEE GRACIA
dc.creatorTAMARIZ MASCARUA, JOAQUIN
dc.creatorGONZALEZ ROMERO, CARLOS
dc.date2018-03-06T15:50:10Z
dc.date2018-03-06T15:50:10Z
dc.date2017-11-15
dc.identifier2090-9071
dc.identifierhttp://hdl.handle.net/20.500.11799/71098
dc.descriptionArtículo Internacional Open Acces
dc.descriptionThe process of N-alkylation of several pyrroles, indoles, and derivative heterocycles is herein described, using quaternary ammonium salts as the source of an alkylating agent. These reactions were carried out on several heterocyclic rings with triethylbenzylammonium chloride or tetradecyltrimethyl ammonium bromide and an NaOH solution at 50%, leading to a chemoselective N-alkylated product and an average yield of 73%. This is an alternative process to the traditional benzylation and methylation of N-heterocycles with direct handling of alkyl halides.
dc.descriptionCONACYT, Secretaría de Investigación y Estudios Avanzados de la UAEM
dc.languageeng
dc.publisherHindawi
dc.rightsopenAccess
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0
dc.subjectN-alkylation
dc.subjectQuaternary Ammonium salts
dc.subjectChemoselective
dc.subjectBIOLOGÍA Y QUÍMICA
dc.titleA novel and chemoselective process of N-alkylation of aromatic nitrogen compounds using quaternary ammonium salts as starting material
dc.typeArtículo
dc.typearticle


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