Issue 15, 1992

Tri-n-butylstannyl radical induced rearrangement of homopropargyl (but-3-ynyl) arenesulfonates: a route to novel 4-aryl-5,6-dihydro-1,2-oxathiin 2,2-dioxides

Abstract

Addition of a tri-n-butylstannyl radical to arenesulfonate esters of the homopropargyl alcohol 1, leads, via ipso-substitution and subsequent 6-endo addition–elimination, to the title derivatives 5.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 1067-1068

Tri-n-butylstannyl radical induced rearrangement of homopropargyl (but-3-ynyl) arenesulfonates: a route to novel 4-aryl-5,6-dihydro-1,2-oxathiin 2,2-dioxides

W. B. Motherwell, A. M. K. Pennell and F. Ujjainwalla, J. Chem. Soc., Chem. Commun., 1992, 1067 DOI: 10.1039/C39920001067

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