Issue 9, 1988

Synthetic approach to medium-sized cycloalkanones. A one-pot three-carbon ring expansion of carbocyclic β-keto esters

Abstract

By treatment with ButOK in Me2SO, carbocyclic β-keto-esters (5-,6-, and 7-membered rings) with a 4-oxopentyl function at the α-position afforded three-carbon ring expansion products (8-, 9-, and 10-membered rings, respectively).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 612-613

Synthetic approach to medium-sized cycloalkanones. A one-pot three-carbon ring expansion of carbocyclic β-keto esters

Z. Xie, H. Suemune and K. Sakai, J. Chem. Soc., Chem. Commun., 1988, 612 DOI: 10.1039/C39880000612

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