Issue 0, 1982

Structure and reactivity of enamines derived from 5,6-dihydro-2H-thiapyran-3(4H)-one 1,1-dioxide

Abstract

The structures and the reactivities of the title vinylogous sulphonamides are compared with those of the corresponding vinylogous amides derived from cyclohexane-1,3-dione. Their behaviour on alkylation, acylation, and addition-substitution has been studied. Isolation of some of the products can be explained in terms of the existence of a tautomeric equilibrium in the parent systems.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 2045-2050

Structure and reactivity of enamines derived from 5,6-dihydro-2H-thiapyran-3(4H)-one 1,1-dioxide

S. Fatutta, G. Pitacco, C. Russo and E. Valentin, J. Chem. Soc., Perkin Trans. 1, 1982, 2045 DOI: 10.1039/P19820002045

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