Palladium-Catalyzed Decarbonylative Nucleophilic Halogenation of Acyl Fluorides and Chlorides: Synthesis of Aryl Halides via Reductive Elimination of the C–X (X = I, Br, and Cl) Bond and Mechanistic Implications-Reference-Cited by-同舟云学术

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Palladium-Catalyzed Decarbonylative Nucleophilic Halogenation of Acyl Fluorides and Chlorides: Synthesis of Aryl Halides via Reductive Elimination of the C–X (X = I, Br, and Cl) Bond and Mechanistic Implications

Published:2024-07-25 Issue:16 Volume:14 Page:11905-11917
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Tian Tian¹,Kashihara Myuto²,Yan Weidan¹,Nishihara Yasushi²^ORCID

Affiliation:

1. Graduate School of Natural Science and Technology, Okayama University, 3-1-1 Tsushimanaka, Kita-ku, 700-8530 Okayama, Japan

2. Research Institute for Interdisciplinary Science (RIIS), Okayama University, 3-1-1 Tsushimanaka, Kita-ku, 700-8530 Okayama, Japan

Funder

China Scholarship Council

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.4c03731

Reference181 articles.

1. The emergence of Pd-mediated reversible oxidative addition in cross coupling, carbohalogenation and carbonylation reactions

2. Theoretical aspects of palladium-catalysed carbon–carbon cross-coupling reactions

3. Modern Transition-Metal-Catalyzed Carbon–Halogen Bond Formation

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