Ir(iii)-Catalyzed direct C–H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2′-amino-1,2′-biaryl scaffolds-Reference-Cited by-同舟云学术

Ir(iii)-Catalyzed direct C–H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2′-amino-1,2′-biaryl scaffolds

Published:2020 Issue:23 Volume:56 Page:3441-3444
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Li Xingjun¹²³⁴⁵,Wang Jiang⁵⁶⁷⁸⁹^ORCID,Xie Xiong⁵⁶⁷⁸⁹,Dai Wenhao¹²³⁴⁵,Han Xu⁵⁶⁷⁸⁹,Chen Kaixian¹²³⁴⁵,Liu Hong¹²³⁴⁵^ORCID

Affiliation:

1. State Key Laboratory of Natural Medicines and Department of Medicinal Chemistry

2. China Pharmaceutical University

3. Nanjing

4. P. R. China

5. State Key Laboratory of Drug Research and Key Laboratory of Receptor Research

6. Shanghai Institute of Materia Medica

7. Chinese Academy of Sciences

8. Shanghai 201203

9. China

Abstract

A novel strategy is reported for the construction of 2-hydroxy-2′-amino-1,1′-biaryl scaffolds via Ir(iii)-catalyzed direct C–H bond activation under mild reaction conditions.

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CC/C9CC08297B

Reference55 articles.

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2. Enantioselective protonation of α-hetero carboxylic acid-derived ketene disilyl acetals under chiral ionic Brønsted acid catalysis

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4. Modified BINOL Ligands in Asymmetric Catalysis

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