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Clean and efficient microwave-solvent-free conversion of homochiral amines, α-amino alcohols and α-amino acids to their chiral 2-substituted pyrrole derivatives

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dc.contributor.authorAydogan, F
dc.contributor.authorDemir, AS
dc.date.accessioned2026-06-27T13:05:08Z
dc.date.issued2005
dc.description.abstractEfficient synthesis of 1,2-disubstituted homochiral pyrroles has been achieved by a two-component coupling of chloroenones and amine compounds on the surface of silica gel without any solvent under microwave irradiation. (c) 2005 Elsevier Ltd. All rights reserved.en
dc.description.urihttps://doi.org/10.1016/j.tet.2005.01.120
dc.identifier.doi10.1016/j.tet.2005.01.120
dc.identifier.eissn1464-5416
dc.identifier.endpage3023
dc.identifier.issn0040-4020
dc.identifier.issue12
dc.identifier.startpage3019
dc.identifier.urihttps://hdl.handle.net/20.500.14981/49496
dc.identifier.volume61
dc.identifier.wos000227754500005
dc.language.isoeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.relation.ispartofTETRAHEDRON
dc.rightsopenAccess
dc.subjectpyrrole
dc.subjectmicrowave
dc.subjectsilica gel
dc.subjectchloroenone
dc.subjectPHOTOOXYGENATION
dc.subjectACYLATION
dc.subjectCHEMISTRY
dc.subjectSYSTEMS
dc.titleClean and efficient microwave-solvent-free conversion of homochiral amines, α-amino alcohols and α-amino acids to their chiral 2-substituted pyrrole derivatives
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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