Issue 4, 1975

Acid-catalysed rearrangement of the 5-bromo-5-methanesulphinylbicyclo-[2,2,1]hept-2-enes

Abstract

The acid-catalysed rearrangement of the nor-bornenyl α-bromo sulphoxides (2) results in a cleavage-recombination sequence ultimately generating the regioselective addition product of dehydronorcamphor and methanesulphenyl bromide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 107-108

Acid-catalysed rearrangement of the 5-bromo-5-methanesulphinylbicyclo-[2,2,1]hept-2-enes

J. C. Philips, M. Penzo and G. T. S. Lee, J. Chem. Soc., Chem. Commun., 1975, 107 DOI: 10.1039/C39750000107

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