Issue 6, 1998

The reductive coupling of tertiary amides to give enediamines using PhMe2SiLi

Abstract

PhMe2SiLi reacts with tertiary amides to give enediamines, which can be isolated in good yield when the α-carbon is branched; the enediamines can be hydrolysed more or less easily to α-amino ketones, isomerised from Z to E, oxidised to dienediamines and isomerised to amino enamines.

Article information

Article type
Paper

Chem. Commun., 1998, 711-712

The reductive coupling of tertiary amides to give enediamines using PhMe2SiLi

I. Fleming, U. Ghosh, S. R. Mack, I. Fleming, U. Ghosh, S. R. Mack and B. P. Clark, Chem. Commun., 1998, 711 DOI: 10.1039/A800648B

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.

Social activity

Spotlight

Advertisements