Issue 44, 2019

Metal-free C–C bond formation via coupling of nitrile imines and boronic acids

Abstract

The challenges of developing sustainable methods of carbon–carbon bond formation remains a topic of considerable importance in synthetic chemistry. Capitalizing on the highly reactive nature of the nitrile imine 1,3-dipole, we have developed a novel metal-free coupling of this species with aryl boronic acids. Photochemical generation of a nitrile imine intermediate and trapping with a palette of boronic acids enabled rapid and facile access to a broad library of more than 25 hydrazone derivatives in up to 92% yield, forming a carbon–carbon bond in a metal free fashion. This represents the first reported example of direct reaction between boronic acids and a 1,3-dipole.

Graphical abstract: Metal-free C–C bond formation via coupling of nitrile imines and boronic acids

Supplementary files

Article information

Article type
Edge Article
Submitted
19 Jun 2019
Accepted
16 Sep 2019
First published
27 Sep 2019
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2019,10, 10412-10416

Metal-free C–C bond formation via coupling of nitrile imines and boronic acids

K. Livingstone, S. Bertrand, J. Mowat and C. Jamieson, Chem. Sci., 2019, 10, 10412 DOI: 10.1039/C9SC03032H

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