Issue 11, 1970

Steroidal analogues of unnatural configuration. Part I. 4,4,14α-Trimethyl-19(10 → 9β)abeo-10α-pregn-5-enes from cucurbitacins

Abstract

An efficient method for the side-chain cleavage of acetylated cucurbitacins with lead tetra-acetate is described. This reaction afforded 4,4,14α-trimethyl-19(10 9β)abeo-10α-pregn-5-ene derivatives of cucurbitacins A, B, C, and E, and further degradation of the cleavage products of cucurbitacins A and B led to A-ring ketones.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 1592-1596

Steroidal analogues of unnatural configuration. Part I. 4,4,14α-Trimethyl-19(10 → 9β)abeo-10α-pregn-5-enes from cucurbitacins

J. R. Bull and K. B. Norton, J. Chem. Soc. C, 1970, 1592 DOI: 10.1039/J39700001592

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