Issue 4, 1991

Preparation of some novel prostanoids based on a tetrahydropyran ring system

Abstract

The prostanoids 31, 33 and 42 have been prepared from tri-O-acetyl-D-glucal 5. The key step in the formation of the prostaglandin analogues 31 and 33 involves the photocatalysed reaction between the thiocarbonate 4 and the allylstannane 21 leading to the stereocontrolled formation of a new carbon–carbon bond through a C-centred radical addition–elimination process.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 787-797

Preparation of some novel prostanoids based on a tetrahydropyran ring system

M. J. Kelly and S. M. Roberts, J. Chem. Soc., Perkin Trans. 1, 1991, 787 DOI: 10.1039/P19910000787

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