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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/123456789/3071
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dc.contributor.authorKumar, Dalip-
dc.date.accessioned2021-10-27T04:22:00Z-
dc.date.available2021-10-27T04:22:00Z-
dc.date.issued2008-01-28-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040403907023933?via%3Dihub-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3071-
dc.description.abstractA simple and efficient synthesis of naturally occurring 5-(3-indolyl)oxazoles is described. The key steps of this convergent approach are the formation of a 3-tosyloxyacetyl-1-benzenesulfonylindole, a 3-amino-acetyl-1-benzenesulfonylindole hydrochloride and cyclodehydration of an α-acylaminoketone.en_US
dc.language.isoenen_US
dc.publisherElsieveren_US
dc.subjectChemistryen_US
dc.subject5-(3-Indolyl)oxazolesen_US
dc.subjectHydroxy(tosyloxy)-iodobenzeneen_US
dc.subjectα-Acylaminoketonesen_US
dc.titleA facile synthesis of naturally occurring 5-(3-indolyl)oxazolesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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