Issue 6, 1975

The benzylidene thiolactone rearrangement: a synthesis of 2-aryl-2,3-dihydrobenzo[b]thiophen-3-carboxylic acids

Abstract

Benzylidene derivatives of benzo[b]thiophen-2-one undergo base-catalysed ring opening and reclosure to produce high yields of 2-aryl-2,3-dihydrobenzo[b]-thiophen-3-carboxylic acids.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 207-208

The benzylidene thiolactone rearrangement: a synthesis of 2-aryl-2,3-dihydrobenzo[b]thiophen-3-carboxylic acids

R. A. Conley and N. Heindel, J. Chem. Soc., Chem. Commun., 1975, 207 DOI: 10.1039/C39750000207

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