Issue 3, 1988

Synthetic approaches to thiathromboxanes. Part 2. Synthesis of structural isomers of thiathromboxane A2

Abstract

Structural isomers (15) of monothiathromboxane A2 have been prepared from the half-ester (1). The basic strategy involved introduction of the ‘bottom’ side-chain by Michael addition, lactonisation, removal of ethoxycarbonyl, and conventional introduction of the ‘top’ side-chain. A link with a published dithiathromboxane synthesis is described.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1988, 675-679

Synthetic approaches to thiathromboxanes. Part 2. Synthesis of structural isomers of thiathromboxane A2

B. P. McDonald, R. W. Steele, J. K. Sutherland, B. W. Leslie and A. Brewster, J. Chem. Soc., Perkin Trans. 1, 1988, 675 DOI: 10.1039/P19880000675

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements