Ligands for Copper-Catalyzed C−N Bond Forming Reactions with 1 Mol% CuBr as Catalyst-Reference-Cited by-同舟云学术

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Ligands for Copper-Catalyzed C−N Bond Forming Reactions with 1 Mol% CuBr as Catalyst

Published:2011-03-22 Issue:9 Volume:76 Page:3151-3159
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yang Kai¹²,Qiu Yatao¹,Li Zheng³,Wang Zhaoyang²,Jiang Sheng¹

Affiliation:

1. Laboratory of Regenerative Biology, Guangzhou, Institute of Biomedicine and Health, CAS, Guangzhou, 510663, People's Republic of China

2. School of Chemistry and Environment, South China Normal University, Guangzhou 510006, People's Republic of China

3. The Methodist Hospital Research Institute, Houston, Texas 77030, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo1026035

Reference76 articles.

1. Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction

2. Modern Synthetic Methods for Copper-Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation

3. Renaissance of Ullmann and Goldberg Reactions - Progress in Copper Catalyzed C-N-, C-O- and C-S-Coupling

4. Copper in cross-coupling reactions

5. Copper-Mediated Coupling Reactions and Their Applications in Natural Products and Designed Biomolecules Synthesis

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2. 7-Azaindole N-Oxide (7-AINO) Mediated Cu-Catalyzed N-Arylation: Mechanistic Investigation into the Role of Fluoride Ions;ACS Catalysis;2023-08-28

3. Bayesian Optimization as a Sustainable Strategy for Early-Stage Process Development? A Case Study of Cu-Catalyzed C–N Coupling of Sterically Hindered Pyrazines;ACS Sustainable Chemistry & Engineering;2023-07-07

4. 3-Substituted Blatter Radicals: Cyclization of N-Arylguanidines and N-Arylamidines to Benzo[e][1,2,4]triazines and PhLi Addition;The Journal of Organic Chemistry;2023-02-17

5. Copper (I) bromide (CuBr): a highly efficient catalyst for the synthesis of β-enaminone derivatives using ultrasound irradiation under solvent-free conditions;Research on Chemical Intermediates;2022-10-13

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