Publication:
Organopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenes

dc.contributor.authorNakin Surapanichen_US
dc.contributor.authorPatcharin Chaisuwanen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.otherRajabhat Rajanagarindra Universityen_US
dc.contributor.otherSuranaree University of Technologyen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-12-11T02:31:45Z
dc.date.accessioned2019-03-14T08:04:26Z
dc.date.available2018-12-11T02:31:45Z
dc.date.available2019-03-14T08:04:26Z
dc.date.issued2016-12-01en_US
dc.description.abstract© Georg Thieme Verlag Stuttgart.New York-Synlett 2016. A formal [3+2] cycloaddition of triphenylcarbenium tetrafluoroborate with structurally different styrene derivatives has been developed. A combination of benzophenone and Et3N is key for promoting a formal [3+2] cycloaddition of triphenylcarbenium tetrafluoroborate with styrenes affording 1,1-diphenyl-3-arylindanes in moderate to good yields. The reaction mechanism of this transformation is also discussed.en_US
dc.identifier.citationSynlett. Vol.27, No.19 (2016), 2689-2694en_US
dc.identifier.doi10.1055/s-0036-1588302en_US
dc.identifier.issn14372096en_US
dc.identifier.issn09365214en_US
dc.identifier.other2-s2.0-84984850896en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/43377
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84984850896&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleOrganopromoted Direct Synthesis of 1,1-Diphenyl-3-arylindanes via Formal [3+2] Cycloadditions of Triphenylcarbenium Tetrafluoroborate with Styrenesen_US
dc.typeReviewen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84984850896&origin=inwarden_US

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