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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3106
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dc.contributor.authorKumar, Dalip-
dc.date.accessioned2021-10-27T04:24:10Z-
dc.date.available2021-10-27T04:24:10Z-
dc.date.issued1998-12-10-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040403998020590?via%3Dihub-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3106-
dc.description.abstractEasily accessible 2-aryl-1,2,3,4-tetrahydro-4-quinolones are readily oxidized to the corresponding 4-alkoxy-2-arylquinolines using a relatively safe hypervalent iodine reagent, [hydroxy (tosyloxy)iodo]benzene (HTIB), in high yields, thus providing a concise route to an important class of naturally occurring alkaloids. 2-Aryl-1,2,3,4-tetrahydro-4-quinolones are readily oxidized to the corresponding 4-alkoxy-2-arylquinolines by [hydroxy(tosyloxy)iodo]benzene(HTIB), thus providing a concise route to a class of naturally occurring alkaloids.en_US
dc.language.isoenen_US
dc.publisherElsieveren_US
dc.subjectChemistryen_US
dc.subjectHypervalenten_US
dc.titleHypervalent iodine oxidation of 2-aryl-1,2,3,4-tetrahydro-4-quinolones: An expedient route to naturally occurring 4-alkoxy-2-arylquinolinesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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