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Showing papers on "Withania somnifera published in 1966"


Journal ArticleDOI
TL;DR: The pyrazole alkaloid (I) has been isolated from the roots of Withania somnifera Dun (Solanaceae), which are used medicinally in India as mentioned in this paper.

75 citations


Journal ArticleDOI
TL;DR: Several Steroidal 5,6expoxy-derivatives bearing an oxygen substituent at C4 have been synthesized and the stereochemistry of rings A and B studied.

18 citations


Journal ArticleDOI
TL;DR: Withaferin A, the steroidal lactone isolated from the leaves of Withania somnifera Dun, has been degraded to bisnor-(5α)-cholanic acid as mentioned in this paper.
Abstract: Withaferin A, the steroidal lactone isolated from the leaves of Withania somnifera Dun. (Solanaceae), has been degraded to bisnor-(5α)-cholanic acid. The β-orientation of the 5,6-epoxide has been demonstrated by optical rotatory dispersion and n.m.r. data. Consequently, withaferin A is a 5β-steroid with the usual stereochemistry at all asymmetric centres, possessing a six-membered-ring lactone in the side-chain.

11 citations


Journal ArticleDOI
TL;DR: In this paper, a new steroidal lactone isomeric with withaferin A has been isolated from the leaves of Withania somnifera Dun, which has been characterised as the title compound.
Abstract: A new steroidal lactone isomeric with withaferin A has been isolated from the leaves of Withania somnifera Dun. It has been characterised as the title compound.

10 citations


Journal ArticleDOI
TL;DR: In this paper, the acid-catalysed rearrangement of the naturally occurring steroidal lactone withaferin A and of some of its derivatives has been investigated and the mass spectra of six significant compounds of this series are discussed.
Abstract: The acid-catalysed rearrangement of the naturally occurring steroidal lactone withaferin A and of some of its derivatives has been investigated. Deoxy-dihydrowithaferin A undergoes a pinacol type rearrangement in which contraction of ring A takes place leading to an A-nor-5-formyl derivative. A similar rearranged product has been obtained by the catalytic hydrogenation of deoxy-dihydrowithaferin A. Under acidic conditions, withaferin A yields, by loss of one ring-A carbon atom, a 2,5-dien-1-one. The mass spectra of six significant compounds of this series are discussed.

5 citations