Issue 1, 1970

Studies of heterocyclic compounds. Part VII. Thioformylindolizines

Abstract

1- and 3-Thioformylindolizines, a class of stable heterocyclic thioaldehydes, have been synthesised by a novel variation of the Vilsmeier reaction. They have also been obtained, in lower yield, by thionation of 1- and 3-formyl-indolizines, and by solvolysis of 3-ethoxymethylene-3H-indolizinium salts with sodium hydrogen sulphide. U.v. and 1H n.m.r. spectral data of the thioaldehydes are discussed.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 145-150

Studies of heterocyclic compounds. Part VII. Thioformylindolizines

S. McKenzie and D. H. Reid, J. Chem. Soc. C, 1970, 145 DOI: 10.1039/J39700000145

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