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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/123456789/3039
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dc.contributor.authorKumar, Dalip-
dc.date.accessioned2021-10-27T04:20:15Z-
dc.date.available2021-10-27T04:20:15Z-
dc.date.issued2014-
dc.identifier.urihttps://www.organic-chemistry.org/abstracts/lit4/497.shtm-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3039-
dc.description.abstractA 2-iodoxybenzoic acid/tetraethylammonium bromide mediated oxidative cyclization of hydrazide-hydrazones generated in situ from aryl glyoxal and hydrazides enables an efficient and high-yielding protocol for the preparation of α-keto-1,3,4-oxadiazoles under mild conditions in short reaction times.en_US
dc.language.isoenen_US
dc.publisherThiemeen_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.titleA Facile and Expeditious One-Pot Synthesis of α-Keto-1,3,4-oxadiazolesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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