Issue 20, 1985

Persistent cation radicals containing carboxamide and thiophosphinic amide functions. The one electron oxidation of acceptor stabilized 1,4-dihydropyrazines

Abstract

Even when it is N,N′-disubstituted by the acceptor groups C(O)Me and P(S) Me2, the 1,4-dihydropyrazine system remains sufficiently electron rich to undergo facile one-electron oxidation to give persistent radical cations with acetamide and thiophosphinic amide functionality.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1369-1370

Persistent cation radicals containing carboxamide and thiophosphinic amide functions. The one electron oxidation of acceptor stabilized 1,4-dihydropyrazines

C. Bessenbacher, R. Gross and W. Kaim, J. Chem. Soc., Chem. Commun., 1985, 1369 DOI: 10.1039/C39850001369

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