Issue 16, 1998

Synthetic approaches to pseudopterosin G aglycone dimethyl ether

Abstract

Three successive reactions of a dimethoxy arene with allylic cation equivalents were used to convert 2,3-dimethoxy-4-methyl-1-iodobenzene to the hexahydro-1H-phenalene system of the potent marine antiinflammatory pseudopterosins G–J.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 2475-2478

Synthetic approaches to pseudopterosin G aglycone dimethyl ether

J. LeBrazidec, P. J. Kocienski, J. D. Connolly and K. W. Muir, J. Chem. Soc., Perkin Trans. 1, 1998, 2475 DOI: 10.1039/A803888K

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