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The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

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

Open access
Shaw, Megan H., Shurtleff, Valerie W., Terrett, Jack A., Cuthbertson, James D., MacMillan, David W. C.·2016·Science

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

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Metadata

Authors
Shaw, M. H., Shurtleff, V. W., Terrett, J. A., Cuthbertson, J. D., & MacMillan, D. W. C.
Venue
Science
Published
2016-06-10
Volume
352
Issue
6291
Pages
1304-1308
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2343326307
Cited by
643
References
1
FWCI
32.67
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Native functionality in triple catalytic cross-coupling: sp 3 C–H bonds as latent nucleophiles. https://app.cochat.ai/papers/10.1126/science.aaf6635
The paper
Shaw, M. H., Shurtleff, V. W., Terrett, J. A., Cuthbertson, J. D., & MacMillan, D. W. C. (2016). Native functionality in triple catalytic cross-coupling: sp 3 C–H bonds as latent nucleophiles. Science. https://doi.org/10.1126/science.aaf6635

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