Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/462
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dc.contributor.authorGirdhar, N Kumar-
dc.contributor.authorFaruk, Abdul-
dc.contributor.authorSuri, K Avtar-
dc.contributor.authorIshar, M P S-
dc.date.accessioned2008-03-24T09:54:01Z-
dc.date.available2008-03-24T09:54:01Z-
dc.date.issued2007-01-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/462-
dc.description192-194en_US
dc.description.abstractUV irradiation of 16⍺,17⍺-epoxy-3β-hydroxypregn-5-ene-20-one 5 in a variety of solvents (benzene, acetonitrile, methanol), as such and in the presence of triethylamine, in a pyrex glass reactor leads to the formation of 3β-hydroxypregn-5-ene-16,20-dione 6 as the major product.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt.Cl. ⁸C07Cen_US
dc.sourceIJCB Vol.46B(1) [January 2007]en_US
dc.subjectSteroidsen_US
dc.subjectphotochemistryen_US
dc.subject⍺-epoxyketoneen_US
dc.subjectphototransformationen_US
dc.subjectβ-diketoneen_US
dc.titlePhototransformation of 16⍺,17 ⍺-epoxy-3β-hydroxypregn- 5-ene-20-one to 3β-hydroxypregn-5-ene-16,20-dioneen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.46B(01) [January 2007]

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