Issue 0, 1981

The synthesis of the 9,11-hydroxyethano-prostaglandin endoperoxide H2 analogue

Abstract

The 9,11-hydroxyethano-prostaglandin endoperoxide H2 analogue (4a) and its methyl ester (4b) have been prepared in 4.3 and 10% yield respectively from the readily prepared 3-exo-methoxycarbonyl-6-endo-hydroxy-5-exo-iodonorborn-2-endo-ylacetic acid δ-lactone (5).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1981, 150-153

The synthesis of the 9,11-hydroxyethano-prostaglandin endoperoxide H2 analogue

S. P. Briggs, D. I. Davies, R. F. Newton and D. P. Reynolds, J. Chem. Soc., Perkin Trans. 1, 1981, 150 DOI: 10.1039/P19810000150

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