CuSO4/N-(9H-carbazol-9-yl)picolinamide-Catalyzed C–O Coupling of (Hetero)Aryl Chlorides with Phenols on Water-Reference-Cited by-同舟云学术

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CuSO₄/N-(9H-carbazol-9-yl)picolinamide-Catalyzed C–O Coupling of (Hetero)Aryl Chlorides with Phenols on Water

Published:2024-08-21 Issue:34 Volume:26 Page:7202-7206
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Hong Peng¹²,Zhu Xinhai²³,Chen Fu¹,Huang Manna¹²^ORCID,Wan Yiqian¹²^ORCID

Affiliation:

1. School of Chemical Engineering and Technology, Sun Yat-sen University, Zhuhai 519082, P. R. China

2. Guangdong Engineering Technology Research Center for Platform Chemicals from Marine Biomass and Their Functionalization, Sun Yat-sen University, Zhuhai 519082, P. R. China

3. Instrument Analysis & Research Center, Sun Yat-sen University, Guangzhou 510275, P. R. China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c02620

Reference45 articles.

1. Oxalohydrazide Ligands for Copper‐Catalyzed C−O Coupling Reactions with High Turnover Numbers

2. Selected Copper-Based Reactions for C−N, C−O, C−S, and C−C Bond Formation

3. Advances in Nickel-Catalyzed O-Arylation of Aliphatic Alcohols and Phenols with (Hetero)aryl Electrophiles

4. Exploration of Nitroaromatic Antibiotics via Sanger’s Reagent: Synthesis, In Silico, and Antimicrobial Evaluation

5. P(i-BuNCH2CH2)3N: An Efficient Promoter for the Nucleophilic Aromatic Substitution Reaction of Aryl Fluorides with Aryl TBDMS (or TMS) Ethers

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