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The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Analysis of the Concerted Metalation-Deprotonation Mechanism in Palladium-Catalyzed Direct Arylation Across a Broad Range of Aromatic Substrates

Gorelsky, Serge I., Lapointe, David, Fagnou, Keith·2008·Journal of the American Chemical Society

Abstract

The concerted metalation-deprotonation mechanism predicts relative reactivity and regioselectivity for a diverse set of arenes spanning the entire spectrum of known palladium-catalyzed direct arylation coupling partners. An analysis following an active strain model provides a more complete portrayal of the important arene/catalyst parameters leading to a successful coupling. The breadth of arenes whose reactivity can be predicted by the CMD mechanism indicates that it may be far more widespread than previously imagined.

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Crossref · 10.1021/ja802533u

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Metadata

Authors
Gorelsky, S. I., Lapointe, D., & Fagnou, K.
Venue
Journal of the American Chemical Society
Published
2008-07-29
Volume
130
Issue
33
Pages
10848-10849
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W1980934047
Cited by
1,009
References
2
FWCI
31.53
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Analysis of the Concerted Metalation-Deprotonation Mechanism in Palladium-Catalyzed Direct Arylation Across a Broad Range of Aromatic Substrates. https://app.cochat.ai/papers/10.1021/ja802533u
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Gorelsky, S. I., Lapointe, D., & Fagnou, K. (2008). Analysis of the Concerted Metalation-Deprotonation Mechanism in Palladium-Catalyzed Direct Arylation Across a Broad Range of Aromatic Substrates. Journal of the American Chemical Society. https://doi.org/10.1021/ja802533u

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.