Issue 5, 1981

Cycloadditions of 3-methoxyfuran with mono-activated dienophiles; application to the synthesis of (±)-avenaciolides

Abstract

Cycloadditions of 3-methoxyfuran (1) with several mono-activated dienophiles gave the endo adducts stereoselectively under the usual conditions in satisfactory yields; two of the adducts were transformed into potential intermediates (7a) and (7b) for the synthesis of (±)-avenaciolide and (±)-isoavenaciolide, respectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 221-222

Cycloadditions of 3-methoxyfuran with mono-activated dienophiles; application to the synthesis of (±)-avenaciolides

A. Murai, K. Takahashi, H. Taketsuru and T. Masamune, J. Chem. Soc., Chem. Commun., 1981, 221 DOI: 10.1039/C39810000221

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