Nickel-Catalyzed Hydrocarboxylation of Terminal Unactivated Alkenes: Formation of Branched Carboxylic Acids and Competing Catalyst Deactivation from CO<sub>2</sub> Reduction to CO-Reference-Cited by-同舟云学术

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Nickel-Catalyzed Hydrocarboxylation of Terminal Unactivated Alkenes: Formation of Branched Carboxylic Acids and Competing Catalyst Deactivation from CO₂ Reduction to CO

Published:2024-06-18 Issue:13 Volume:43 Page:1502-1510
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Khamespanah Fatemeh¹,Gerken James B.¹^ORCID,Mannel David S.²,Nagy Sandor²,Kimmich Barbara²,Stahl Shannon S.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Wisconsin−Madison, 1101 University Avenue, Madison, Wisconsin 53706, United States

2. Houston Technology Center, LyondellBasell, 8280 Sheldon Road, Channelview, Texas 77530, United States

Funder

National Institute of General Medical Sciences

National Science Foundation

LyondellBasell

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.4c00218

Reference48 articles.

1. Carboxylic Acids, Aliphatic

2. Transition‐Metal‐Catalyzed Carboxylation Reactions with Carbon Dioxide

3. Transition metal-catalyzed carboxylation of unsaturated substrates with CO2

4. Transition metal-mediated or catalyzed hydrocarboxylation of olefins with CO2

5. New nickel–carbon dioxide complex: synthesis, properties, and crystallographic characterization of (carbon dioxide)-bis(tricyclohexylphosphine)nickel

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