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Cited by 277

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

Full Selectivity Control in Cobalt(III)‐Catalyzed C−H Alkylations by Switching of the C−H Activation Mechanism

Zell, Daniel, Bursch, Markus, Müller, Valentin, Grimme, Stefan, Ackermann, Lutz·2017·Angewandte Chemie International Edition

Abstract

Selectivity control in hydroarylation‐based C−H alkylation has been dominated by steric interactions. A conceptually distinct strategy that exploits the programmed switch in the C−H activation mechanism by means of cobalt catalysis is presented, which sets the stage for convenient C−H alkylations with unactivated alkenes. Detailed mechanistic studies provide compelling evidence for a programmable switch in the C−H activation mechanism from a linear‐selective ligand‐to‐ligand hydrogen transfer to a branched‐selective base‐assisted internal electrophilic‐type substitution.

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Metadata

Authors
Zell, D., Bursch, M., Müller, V., Grimme, S., & Ackermann, L.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2017-07-24
Volume
56
Issue
35
Pages
10378-10382
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2635391339
Cited by
277
References
1
FWCI
17.36
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Full Selectivity Control in Cobalt(III)‐Catalyzed C−H Alkylations by Switching of the C−H Activation Mechanism. https://app.cochat.ai/papers/10.1002/anie.201704196
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Zell, D., Bursch, M., Müller, V., Grimme, S., & Ackermann, L. (2017). Full Selectivity Control in Cobalt(III)‐Catalyzed C−H Alkylations by Switching of the C−H Activation Mechanism. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201704196

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