Issue 23, 1976

Prostaglandins. Part 4. Synthesis of (±)-11-deoxyprostaglandins from 2-(ω-hydroxyheptyl)cyclopent-2-enones

Abstract

Conjugate nitrile addition to 2-(7-hydroxyheptyl)cyclopent-2-enone (IIIa) and subsequent elaboration via the aldehydes [(VIa), (Xa)] affords a convenient direct route to (±)-11-deoxyprostaglandins of the E1 and F1 series. Syntheses of (±)-10-methyl- and (±)-α-nor-11-deoxyprostaglandins are also described.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1976, 2550-2556

Prostaglandins. Part 4. Synthesis of (±)-11-deoxyprostaglandins from 2-(ω-hydroxyheptyl)cyclopent-2-enones

T. S. Burton, M. P. L. Caton, E. C. J. Coffee, T. Parker, K. A. J. Stuttle and G. L. Watkins, J. Chem. Soc., Perkin Trans. 1, 1976, 2550 DOI: 10.1039/P19760002550

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