Issue 9, 2014

Reductive decyanation of malononitriles and cyanoacetates using photoactivated neutral organic super-electron-donors

Abstract

A metal-free reductive procedure for decyanation of malononitriles and cyanoacetates, using photoactivated organic electron donors, is described. Decyanation of cyanoacetates is more difficult than for malononitriles and it requires higher loading of the electron donor and extended reaction times. An anionic intermediate is proposed for the observed decyanations and a plausible mechanism is presented.

Graphical abstract: Reductive decyanation of malononitriles and cyanoacetates using photoactivated neutral organic super-electron-donors

Supplementary files

Article information

Article type
Research Article
Submitted
24 رمضان 1435
Accepted
25 شوال 1435
First published
29 شوال 1435

Org. Chem. Front., 2014,1, 1072-1076

Author version available

Reductive decyanation of malononitriles and cyanoacetates using photoactivated neutral organic super-electron-donors

E. Doni and J. A. Murphy, Org. Chem. Front., 2014, 1, 1072 DOI: 10.1039/C4QO00202D

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