Issue 0, 1986

General synthetic route to γ-butyrolactones via stereoselective radical cyclization by organotin species

Abstract

A new method for the preparation of γ-butyrolactones is described in which the key step is the highly stereoselective radical cyclization of bromoacetals to 2-alkoxytetrahydrofurans in the presence of polymeric or low-molecular weight organotin species. 2-Alkoxytetrahydrofurans can be easily converted into γ-butyrolactones by Jones oxidation.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1986, 1351-1356

General synthetic route to γ-butyrolactones via stereoselective radical cyclization by organotin species

Y. Ueno, O. Moriya, K. Chino, M. Watanabe and M. Okawara, J. Chem. Soc., Perkin Trans. 1, 1986, 1351 DOI: 10.1039/P19860001351

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