Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/71398
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dc.contributor.authorMookda Pattarawarapanen_US
dc.contributor.authorNittaya Wiriyaen_US
dc.contributor.authorSurat Hongsibsongen_US
dc.contributor.authorWong Phakhodeeen_US
dc.date.accessioned2021-01-27T03:42:53Z-
dc.date.available2021-01-27T03:42:53Z-
dc.date.issued2020-12-04en_US
dc.identifier.issn15206904en_US
dc.identifier.issn00223263en_US
dc.identifier.other2-s2.0-85097897981en_US
dc.identifier.other10.1021/acs.joc.0c02403en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85097897981&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/71398-
dc.description.abstract© 2020 American Chemical Society A novel phosphonium-mediated reaction of isatins is described. In the presence of alcohol, the reaction proceeds to furnish C-12 modified tryptanthrin derivatives. Without alcohol, self-dimerization of isatins gives rise to tryptanthrin and its analogs. This divergent and step-economic approach provides a facile access to diverse indoloquinazoline structures including the natural alkaloids, methylisatoid and cephalanthrin B, in high yields from simple precursors under mild and metal-free reaction conditions.en_US
dc.subjectChemistryen_US
dc.titleDivergent Synthesis of Methylisatoid and Tryptanthrin Derivatives by Ph<inf>3</inf>P-I<inf>2</inf>-Mediated Reaction of Isatins with and without Alcoholsen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Organic Chemistryen_US
article.volume85en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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