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Azide-Triggered Bicyclization of o-Alkynylisocyanobenzenes: Synthesis of Tetrazolo[1,5-a]quinolines

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dc.contributor.authorOnnicha Khaikateen_US
dc.contributor.authorDarunee Soorukramen_US
dc.contributor.authorPawaret Leowanawaten_US
dc.contributor.authorManat Pohmakotren_US
dc.contributor.authorVichai Reutrakulen_US
dc.contributor.authorChutima Kuhakarnen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2020-01-27T08:09:57Z
dc.date.available2020-01-27T08:09:57Z
dc.date.issued2019-11-14en_US
dc.description.abstract© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim An efficient and rapid synthetic approach for the synthesis of tetrazolo[1,5-a]quinolines has been developed employing the reaction of o-alkynylisocyanobenzenes with sodium azide. The present strategy involved nucleophilic addition of azide to isocyanide followed by 6-endo cyclization. The reaction gives access to a collection of tetrazolo[1,5-a]quinolines with broad functional group in moderate to high yields under metal-, and base-free conditions.en_US
dc.identifier.citationEuropean Journal of Organic Chemistry. Vol.2019, No.42 (2019), 7050-7057en_US
dc.identifier.doi10.1002/ejoc.201901209en_US
dc.identifier.issn10990690en_US
dc.identifier.issn1434193Xen_US
dc.identifier.other2-s2.0-85074416371en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/50547
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85074416371&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleAzide-Triggered Bicyclization of o-Alkynylisocyanobenzenes: Synthesis of Tetrazolo[1,5-a]quinolinesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85074416371&origin=inwarden_US

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