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Facile and economical Miyaura borylation and one-pot Suzuki–Miyaura cross-coupling reaction

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dc.contributor.authorPhongsakorn Boontiemen_US
dc.contributor.authorSupavadee Kiatisevien_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2020-03-26T04:37:51Z
dc.date.available2020-03-26T04:37:51Z
dc.date.issued2020-06-01en_US
dc.description.abstract© 2020 Elsevier B.V. Facile and economical method for Miyaura borylation reaction between B2pin2 and aryl bromides is reported. The catalytic system containing 2 mol% PdCl2(PPh3)2 and KOAc serves to enable borylations to occur under solvent-free and atmospheric conditions. The developed protocol can be applied to synthesize symmetrical and unsymmetrical biaryls via one-pot two-step Suzuki–Miyaura cross-coupling reaction and also offers the up-scalability.en_US
dc.identifier.citationInorganica Chimica Acta. Vol.506, (2020)en_US
dc.identifier.doi10.1016/j.ica.2020.119538en_US
dc.identifier.issn00201693en_US
dc.identifier.other2-s2.0-85080088425en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/53637
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85080088425&origin=inwarden_US
dc.subjectChemistryen_US
dc.subjectMaterials Scienceen_US
dc.titleFacile and economical Miyaura borylation and one-pot Suzuki–Miyaura cross-coupling reactionen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85080088425&origin=inwarden_US

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