Mixed-Ligand Approach to Palladium-Catalyzed Direct Arylation of Heteroarenes with Aryl Chlorides: Controlling Reactivity of Catalytic Intermediates via Dynamic Ligand Exchange-Reference-Cited by-同舟云学术

Mixed-Ligand Approach to Palladium-Catalyzed Direct Arylation of Heteroarenes with Aryl Chlorides: Controlling Reactivity of Catalytic Intermediates via Dynamic Ligand Exchange

Published:2023-11-21 Issue:24 Volume:42 Page:3454-3465
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Wakioka Masayuki¹²^ORCID,Hatakeyama Keisuke¹³,Sakai Shunta¹³,Seki Takehito¹,Tada Ken-ichi¹,Mizuhata Yoshiyuki²^ORCID,Nakazato Takumi⁴,Koguchi Shinichi⁵^ORCID,Shibuya Yuga⁶,Maruyama Yooichiroh⁴,Ayabe Masatsugu⁴

Affiliation:

1. Sagami Chemical Research Institute, 2743-1 Hayakawa, Ayase, Kanagawa 252-1193, Japan

2. Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan

3. School of Science, Kitasato University, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa 252-0373, Japan

4. JSR Corporation, 100 Kawajiricho, Yokkaichi, Mie 510-8552, Japan

5. Department of Chemistry, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292, Japan

6. Institute of Advanced Biosciences, Tokai University, 4-1-1 Kitakaname, Hiratsuka, Kanagawa 259-1292, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.3c00409

Reference60 articles.

1. Mixed-Ligand Catalysts: A Powerful Tool in Transition-Metal-Catalyzed Cross-Coupling Reactions

2. Serial Ligand Catalysis: A Highly Selective Allylic C−H Oxidation

3. A Multiligand Based Pd Catalyst for C−N Cross-Coupling Reactions

4. Dynamic multiligand catalysis: A polar to radical crossover strategy expands alkyne carboboration to unactivated secondary alkyl halides

5. A relay catalysis strategy for enantioselective nickel-catalyzed migratory hydroarylation forming chiral α-aryl alkylboronates

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