Issue 0, 1974

Preparation and decomposition of some steroidal 4′β,5′-dihydro-[17α,16-c]pyrazoles

Abstract

Reaction of a series of aliphatic diazo-compounds with Δ16-20-oxo-steroids has given the corresponding 4′,5′-dihydro-[17α,16α-c]pyrazoles ([17α,16α-c]pyrazolines). Pyrolysis of the pyrazolines gave in the cases where the substituent on the heterocyclic ring is unsaturated, the 1′β,3′-dihydrocyclopropa[16,17α]-compounds (8) and (9). Pyrolysis of the pyrazolines with a saturated substituent on the heterocyclic ring gave a mixture of the Δ16-16-alkyl- and the 1′β,3′-dihydrocyclopropa[16,17α]-compounds. Photolytic decomposition of the pyrazolines gave only the cyclopropa[16α,17α]-compounds.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 1468-1475

Preparation and decomposition of some steroidal 4′β,5′-dihydro-[17α,16-c]pyrazoles

P. Bladon, D. R. Rae and A. D. Tait, J. Chem. Soc., Perkin Trans. 1, 1974, 1468 DOI: 10.1039/P19740001468

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