Indium triflate catalyzed microwave-assisted alkenylation of methoxyphenols: synthesis of indenes and chromenes

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dc.contributor.authorKumar, Anil
dc.date.accessioned2021-10-17T13:56:05Z
dc.date.available2021-10-17T13:56:05Z
dc.date.issued2015
dc.description.abstractIn(OTf)3 catalyzed microwave-assisted alkenylation of methoxyphenols was investigated. Exclusive formation of either indenes or chromenes was observed depending on the position of the methoxy group on phenol. The structures of 1H-inden-4-ol derivatives (4a–e) and 4H-chromene derivatives (5a–j) were established by NMR (1H & 13C) and high-resolution mass spectra, which were further supported by single crystal X-ray analysis of 4c and 5a.en_US
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2015/OB/C5OB01734C
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2854
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectIndium triflateen_US
dc.subjectMicrowave-assisteden_US
dc.subjectMethoxyphenolsen_US
dc.subjectChromenesen_US
dc.titleIndium triflate catalyzed microwave-assisted alkenylation of methoxyphenols: synthesis of indenes and chromenesen_US
dc.typeArticleen_US

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