Transition‐Metal‐Free C(sp 2 )–C(sp 2 ) Cross‐Coupling of Diazo Quinones with Catechol Boronic Esters-Reference-Cited by-同舟云学术

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Transition‐Metal‐Free C(sp 2 )–C(sp 2 ) Cross‐Coupling of Diazo Quinones with Catechol Boronic Esters

Published:2020-07-14 Issue:37 Volume:132 Page:16336-16342
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Wu Kai¹²^ORCID,Wu Liang‐Liang¹^ORCID,Zhou Cong‐Ying¹²³^ORCID,Che Chi‐Ming¹²^ORCID

Affiliation:

1. State Key Laboratory of Synthetic Chemistry Department of Chemistry The University of Hong Kong Pokfulam Road Hong Kong China

2. HKU Shenzhen Institute of Research & Innovation Shenzhen China

3. Present address: College of Chemistry and Materials Science Jinan University Guangzhou China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202006542

Reference79 articles.

1. “Quinone Diazides”:

2. Structure and Spectroscopic Properties of p ‐Benzoquinone Diazides

3. For selected examples of C−H functionalization see:

4. Cp*Rh(iii) and Cp*Ir(iii)-catalysed redox-neutral C–H arylation with quinone diazides: quick and facile synthesis of arylated phenols

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1. Mechanism of Asymmetric Homologation of Alkenylboronic Acids with CF₃-Diazomethane via Borotropic Rearrangement;The Journal of Organic Chemistry;2024-03-25

2. Selective Formal Carbene Insertion into Carbon‐Boron Bonds of Diboronates by N ‐Trisylhydrazones;Angewandte Chemie International Edition;2023-01-24

3. Selective Formal Carbene Insertion into Carbon‐Boron Bonds of Diboronates by N ‐Trisylhydrazones;Angewandte Chemie;2023-01-24

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