Issue 14, 1977

A synthon for epoxyolefin cyclisation

Abstract

An efficient synthesis of 1,2-epoxy-1-methyl-2-(3-oxopropyl)-4,4-ethylenedioxycyclohexane from 6-methoxy-2-tetralone is described; this aldehyde undergoes Wittig–Schlosser condensation to give epoxyolefins which are possible substrates for epoxyolefin cyclisation.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 497-498

A synthon for epoxyolefin cyclisation

D. Johnson, J. W. Smart and J. K. Sutherland, J. Chem. Soc., Chem. Commun., 1977, 497 DOI: 10.1039/C39770000497

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