Issue 18, 1983

Reaction of tributyltin enolates with α-halogeno ketones: a new route to furan derivatives

Abstract

The reaction of tributyltin enolates with α-halogeno ketones gave substituted furans which were not derived from the normal cross-coupling products, 1,4-diketones, but were formed instead through addition of the tin enolate to the α-halogeno ketones.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 989-990

Reaction of tributyltin enolates with α-halogeno ketones: a new route to furan derivatives

M. Kosugi, I. Takano, I. Hoshino and T. Migita, J. Chem. Soc., Chem. Commun., 1983, 989 DOI: 10.1039/C39830000989

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