Issue 1, 2015

Reductive functionalization of CO2 with amines: an entry to formamide, formamidine and methylamine derivatives

Abstract

CO2 utilization for the production of C1-containing molecules is a desirable route to value-added chemicals. In this perspective, we summarize the recent results devoted to the formation of nitrogen compounds obtained by reductive functionalization of CO2 in the presence of amines. Using mild reductants, such as molecular hydrogen, hydrosilanes and hydroboranes, novel catalytic reactions have been designed in the last few years to facilitate the reductive functionalization of CO2 to formamide, formamidine and methylamine derivatives. While early efforts were devoted to the formylation of N–H bonds, efficient organic and metal catalysts have been developed lately to promote the complete deoxygenation of CO2 to benzimidazoles, quinazolinones, formamidines and methylamines. Finally, the opportunities and challenges facing the practical use of CO2 in the production of nitrogen-containing molecules are discussed.

Graphical abstract: Reductive functionalization of CO2 with amines: an entry to formamide, formamidine and methylamine derivatives

Article information

Article type
Perspective
Submitted
20 авг 2014
Accepted
23 окт 2014
First published
23 окт 2014

Green Chem., 2015,17, 157-168

Author version available

Reductive functionalization of CO2 with amines: an entry to formamide, formamidine and methylamine derivatives

A. Tlili, E. Blondiaux, X. Frogneux and T. Cantat, Green Chem., 2015, 17, 157 DOI: 10.1039/C4GC01614A

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