Issue 78, 2014

Catalytic constructive deoxygenation of lignin-derived phenols: new C–C bond formation processes from imidazole-sulfonates and ether cleavage reactions

Abstract

As part of a programme aimed at exploiting lignin as a chemical feedstock for less oxygenated fine chemicals, several catalytic C–C bond forming reactions utilising guaiacol imidazole sulfonate are demonstrated. These include the cross-coupling of a Grignard, a non-toxic cyanide source, a benzoxazole, and nitromethane. A modified Meyers reaction is used to accomplish a second constructive deoxygenation on a benzoxazole functionalised anisole.

Graphical abstract: Catalytic constructive deoxygenation of lignin-derived phenols: new C–C bond formation processes from imidazole-sulfonates and ether cleavage reactions

Supplementary files

Article information

Article type
Communication
Submitted
27 Jun 2014
Accepted
12 Aug 2014
First published
12 Aug 2014
This article is Open Access
Creative Commons BY license

Chem. Commun., 2014,50, 11511-11513

Author version available

Catalytic constructive deoxygenation of lignin-derived phenols: new C–C bond formation processes from imidazole-sulfonates and ether cleavage reactions

S. M. Leckie, G. J. Harkness and M. L. Clarke, Chem. Commun., 2014, 50, 11511 DOI: 10.1039/C4CC04939J

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