Issue 6, 1993

Unexpected acid-catalysed rearrangement of a vinylcyclopropane derivative

Abstract

A vinylcyclopropane carboxylic acid derivative undergoes a novel type of rearrangement under mild acidic conditions; X-ray diffraction study of the rearrangement product confirms the structure as (1SR,4SR,7SR)-4-methyl-3,9-dioxabicyclo[5.3.0]dec-5-ene-2,10-dione.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 491-492

Unexpected acid-catalysed rearrangement of a vinylcyclopropane derivative

A. M. P. Koskinen, L. Muñoz and K. Rissanen, J. Chem. Soc., Chem. Commun., 1993, 491 DOI: 10.1039/C39930000491

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