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Sulfinates and thiocyanates triggered 6-endo cyclization of o-alkynylisocyanobenzenes

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dc.contributor.authorOnnicha Khaikateen_US
dc.contributor.authorJatuporn Meesinen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorPawaret Leowanawaten_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2019-08-23T10:38:30Z
dc.date.available2019-08-23T10:38:30Z
dc.date.issued2018-01-01en_US
dc.description.abstract© The Royal Society of Chemistry. Diverse 2-sulfonyl- and 2-thiocyanato-3-substituted quinolines were synthesized from o-alkynylisocyanobenzenes by nucleophilic addition of the respective sulfinate sodium salts and ammonium thiocyanate to the isocyanide moiety followed by cyclization. The salient features of the methodology include metal-free, ambient temperature and mild reaction conditions, ease of reagent handling, and broad functional group tolerance.en_US
dc.identifier.citationOrganic and Biomolecular Chemistry. Vol.16, No.44 (2018), 8553-8558en_US
dc.identifier.doi10.1039/C8OB02338Gen_US
dc.identifier.issn14770520en_US
dc.identifier.other2-s2.0-85056520766en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/45272
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85056520766&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleSulfinates and thiocyanates triggered 6-endo cyclization of o-alkynylisocyanobenzenesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85056520766&origin=inwarden_US

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