Issue 4, 1984

The crystal structure of some 2-oxo-1,3,2-dioxathiolanes

Abstract

The trans diastereoisomers of 2-oxo-4(S)-phenyl-1,3,2-dioxathiolane and meso-2-oxo-4,5-diphenyl-1,3,2-dioxathiolane have been unambiguously identified by X-ray analysis; both adopt the half-chair conformation an differential endocyclic S–O bond lengths provide evidence for a stereoelectronic interaction with the S[double bond, length half m-dash]O group.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 262-263

The crystal structure of some 2-oxo-1,3,2-dioxathiolanes

G. Lowe, S. J. Salamone and R. H. Jones, J. Chem. Soc., Chem. Commun., 1984, 262 DOI: 10.1039/C39840000262

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