Issue 15, 1986

Trigonal configuration of disulphonyl carbanions

Abstract

One-bond C–H coupling constants of the anionic carbon of anions derived from disulphones (1)–(3) provide unequivocal evidence for the trigonal hybridization of the charged carbon, previously assigned as tetrahedral; it is shown that the 1,3-dithiolane 1,1,3,3-tetraoxide undergoes ring opening upon treatment with strong bases.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 1191-1192

Trigonal configuration of disulphonyl carbanions

A. Berlin, S. Bradamante, R. Ferraccioli and G. A. Pagani, J. Chem. Soc., Chem. Commun., 1986, 1191 DOI: 10.1039/C39860001191

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