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TBAI/TBHP-Mediated Cascade Cyclization toward Sulfonylated Indeno[1,2-c]quinolines

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dc.contributor.authorJatuporn Meesinen_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorPawaret Leowanawaten_US
dc.contributor.authorSaowanit Saithongen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherPrince of Songkla Universityen_US
dc.date.accessioned2018-12-21T06:36:50Z
dc.date.accessioned2019-03-14T08:02:42Z
dc.date.available2018-12-21T06:36:50Z
dc.date.available2019-03-14T08:02:42Z
dc.date.issued2017-12-15en_US
dc.description.abstract© 2017 American Chemical Society. Treatment of ortho-amino-substituted aryldiyne derivatives with sulfonyl hydrazides in the presence of tetrabutylammonium iodide (TBAI) and tert-butyl hydroperoxide (TBHP) led to a cascade cyclization reaction to yield sulfonylated indeno[1,2-c]quinolines in moderate to good yields. The features of the methodology include metal-free reaction, the ease of reagent handling, and a broad functional group tolerance.en_US
dc.identifier.citationOrganic Letters. Vol.19, No.24 (2017), 6546-6549en_US
dc.identifier.doi10.1021/acs.orglett.7b03246en_US
dc.identifier.issn15237052en_US
dc.identifier.issn15237060en_US
dc.identifier.other2-s2.0-85038411952en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/41727
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85038411952&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleTBAI/TBHP-Mediated Cascade Cyclization toward Sulfonylated Indeno[1,2-c]quinolinesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85038411952&origin=inwarden_US

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