A catalyst- and solvent-free three-component reaction for the regioselective one-pot access to polyfunctionalized pyrroles

Simple item page
dc.contributor.authorBhat, S.I.
dc.contributor.authorTrivedi, D.R.
dc.date.accessioned2026-02-05T09:34:41Z
dc.date.issued2013
dc.description.abstractA facile method for the regioselective synthesis of tetrasubstituted pyrroles, from readily accessible 1,3-dicarbonyls, benzoin derivatives and ammonium acetate, has been developed. The one-pot three-component reactions were performed to afford tetrasubstituted pyrroles under solvent- and catalyst-free conditions. © 2013 Elsevier Ltd. All rights reserved.
dc.identifier.citationTetrahedron Letters, 2013, 54, 41, pp. 5577-5582
dc.identifier.issn404039
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2013.07.153
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/26716
dc.subjectammonium acetate
dc.subjectbenzoin
dc.subjectcarbonyl derivative
dc.subjectpyrrole derivative
dc.subjectarticle
dc.subjectcatalyst
dc.subjectchemical reaction
dc.subjectstereochemistry
dc.subjectsynthesis
dc.titleA catalyst- and solvent-free three-component reaction for the regioselective one-pot access to polyfunctionalized pyrroles

Files

Collections

Journal Articles