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Manganese‐Catalyzed Hydrogen‐Autotransfer C−C Bond Formation: α‐Alkylation of Ketones with Primary Alcohols

Peña‐López, Miguel, Piehl, Patrick, Elangovan, Saravanakumar, Neumann, Helfried, Beller, Matthias·2016·Angewandte Chemie International Edition

Abstract

A novel catalytic hydrogen‐autotransfer protocol for the atom‐efficient α‐alkylation of ketones with readily available alcohols is presented. The use of manganese complexes bearing non‐innocent PNP pincer ligands enabled the functionalization of a broad range of valuable ketones, including 2‐oxindole, estrone 3‐methyl ether, and testosterone. Mechanistic investigations suggest the participation of an intramolecular amidate‐assisted alcohol‐dehydrogenation process.

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Metadata

Authors
Peña‐López, M., Piehl, P., Elangovan, S., Neumann, H., & Beller, M.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2016-10-27
Volume
55
Issue
48
Pages
14967-14971
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2542930749
Cited by
341
References
0
FWCI
19.07
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Manganese‐Catalyzed Hydrogen‐Autotransfer C−C Bond Formation: α‐Alkylation of Ketones with Primary Alcohols. https://app.cochat.ai/papers/10.1002/anie.201607072
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Peña‐López, M., Piehl, P., Elangovan, S., Neumann, H., & Beller, M. (2016). Manganese‐Catalyzed Hydrogen‐Autotransfer C−C Bond Formation: α‐Alkylation of Ketones with Primary Alcohols. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201607072

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