Issue 16, 1974

A stable thio-analogue of a Meisenheimer complex via a spiroannelation route: requirements for annelating chain length

Abstract

2-Picrylthioethane-1-thiol undergoes exclusive intramolecular cyclization to give a crystalline spiro thio-analogue of a Meisenheimer complex under the action of a base, whereas nitro group replacement by thiolate occurs with the propanedithiol analogue.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 672-673

A stable thio-analogue of a Meisenheimer complex via a spiroannelation route: requirements for annelating chain length

E. Farina, C. A. Veracini and F. Pietra, J. Chem. Soc., Chem. Commun., 1974, 672 DOI: 10.1039/C39740000672

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