Publication:
Iodine-catalyzed Friedel-Crafts alkylation of electron-rich arenes with aldehydes: efficient synthesis of triarylmethanes and diarylalkanes

dc.contributor.authorJaray Jaratjaroonphongen_US
dc.contributor.authorSupaporn Sathalalaien_US
dc.contributor.authorPrapapan Techasauvapaken_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.otherFaculty of Scienceen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-13T06:21:17Z
dc.date.available2018-09-13T06:21:17Z
dc.date.issued2009-11-04en_US
dc.description.abstractIodine is shown to be an efficient catalyst for the Friedel-Crafts alkylation of arenes with a wide variety of aldehydes in toluene under 'open-flask' and mild conditions. In the presence of 10 mol % of iodine, the reaction of arenes with aromatic aldehydes gives the corresponding triarylmethane derivatives (TRAMs), regioselectively, in good to excellent yields. On the other hand, a series of diarylalkane derivatives is synthesized smoothly by the reaction with aliphatic aldehydes. © 2009 Elsevier Ltd. All rights reserved.en_US
dc.identifier.citationTetrahedron Letters. Vol.50, No.44 (2009), 6012-6015en_US
dc.identifier.doi10.1016/j.tetlet.2009.08.036en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-70149089461en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/27119
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70149089461&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleIodine-catalyzed Friedel-Crafts alkylation of electron-rich arenes with aldehydes: efficient synthesis of triarylmethanes and diarylalkanesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=70149089461&origin=inwarden_US

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