Palladium-Catalyzed <i>ipso</i>-Borylation of Aryl Halides Promoted by Lewis Acid-Mediated Electrophilic Activation of Aryl(halo)palladium(II) Complex-Reference-Cited by-同舟云学术

Palladium-Catalyzed ipso-Borylation of Aryl Halides Promoted by Lewis Acid-Mediated Electrophilic Activation of Aryl(halo)palladium(II) Complex

Published:2023-11-08 Issue:45 Volume:25 Page:8173-8177
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Niwa Takashi¹²³^ORCID,Takimoto Tadashi¹,Sakata Yuki²,Hosoya Takamitsu¹²^ORCID

Affiliation:

1. Laboratory for Chemical Biology, RIKEN Center for Biosystems Dynamics Research (BDR), 6-7-3 Minatojima-minamimachi, Chuo-ku, Kobe 650-0047, Japan

2. Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU), 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan

3. Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan

Funder

Osaka University

Ministry of Education, Culture, Sports, Science and Technology

RIKEN

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Mitsubishi Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c03531

Reference29 articles.

1. Boron as a key component for new π-electron materials

2. Designs of Functional π-Electron Materials based on the Characteristic Features of Boron

3. Electron‐Deficient Conjugated Materials via p–π* Conjugation with Boron: Extending Monomers to Oligomers, Macrocycles, and Polymers

4. π‐Conjugated Materials Derived From Boron‐Chalcogenophene Combination. A Brief Description of Synthetic Routes and Optoelectronic Applications

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