Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16328
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dc.contributor.authorBoruah, Romesh C-
dc.contributor.authorAhmed, Shahadat-
dc.contributor.authorSharma, Utpal-
dc.contributor.authorSandhu, Jagir S-
dc.date.accessioned2013-03-09T11:21:55Z-
dc.date.available2013-03-09T11:21:55Z-
dc.date.issued1999-03-
dc.identifier.urihttp://hdl.handle.net/123456789/16328-
dc.description274-282en_US
dc.description.abstractA novel class of β -formylsteroidal enamides has been prepared from 16-dehydropregnenolone-20-oxime. Reaction of these enamides with Vilsmeier reagent affords steroidal geminal dichlorides in good yields. Reaction of the corresponding C-16 formylidenemalononitrile derivative with chloromethyleneiminium salt, however, leads to a ring-D fused pyridosteroid.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.38B(03) [March 1999]en_US
dc.titleSynthesis of β-formylsteroidal enamides and their conversion into geminal dichloridesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(03) [March 1999]

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