Native functionality in triple catalytic cross-coupling: sp 3 C–H bonds as latent nucleophiles

Author:

Shaw Megan H.1,Shurtleff Valerie W.1,Terrett Jack A.1,Cuthbertson James D.1,MacMillan David W. C.1

Affiliation:

1. Merck Center for Catalysis at Princeton University, Princeton, NJ 08544, USA.

Abstract

A tip of the HAT to C-C bond formation Iridium and nickel are already a proven team for forging carbon-carbon bonds. The iridium harvests blue light from a simple light-emitting diode and orchestrates the coupling by the nickel. Shaw et al. now add a third player to the team, a hydrogen atom transfer (HAT) catalyst (see the Perspective by Fruit). Together, the trio of catalysts can link bromo- or chloroaryl rings directly to C-H sites adjacent to nitrogen or oxygen, with no need for prior modification. The reaction is highly selective across a broad range of substrates. Science , this issue p. 1304 ; see also p. 1277

Funder

NIH National Institute of General Medical Sciences

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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