Issue 21, 1990

Intramolecular oxidative cyclisation of 5-stannyl-1,3-pentanediol derivatives with lead tetra-acetate

Abstract

The oxidative cyclisation of 5-stannyl-1,3-pentanediol derivatives gave corresponding 4-hydroxytetrahydropyrans in excellent yields, and its applications to the synthesis of dioxabicyclodecane 12 and 4-hydroxy-δ-lactone 14 are also described.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1492-1493

Intramolecular oxidative cyclisation of 5-stannyl-1,3-pentanediol derivatives with lead tetra-acetate

M. Yamamoto, S. Irie, T. Arase, S. Kohmoto and K. Yamada, J. Chem. Soc., Chem. Commun., 1990, 1492 DOI: 10.1039/C39900001492

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