Nickel‐Catalyzed Amination of (Hetero)aryl Halides Facilitated by a Catalytic Pyridinium Additive-Reference-Cited by-同舟云学术

Nickel‐Catalyzed Amination of (Hetero)aryl Halides Facilitated by a Catalytic Pyridinium Additive

Published:2020-09-03 Issue:54 Volume:26 Page:12349-12354
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Han Dongyang¹^ORCID,Li Sasa¹^ORCID,Xia Siqi²^ORCID,Su Mincong²^ORCID,Jin Jian¹^ORCID

Affiliation:

1. CAS Key Laboratory of Synthetic Chemistry of Natural Substances Center for Excellence in Molecular Synthesis Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences, Chinese Academy of Sciences 345 Lingling Road Shanghai 200032 P. R. China

2. Center for Supramolecular Chemistry and Catalysis Department of Chemistry College of Sciences Shanghai University 99 Shangda Road Shanghai 200444 P. R. China

Funder

Natural Science Foundation of Shanghai

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202002800

Reference79 articles.

1. Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?

3. Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides

4. Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions

5. The 25th Anniversary of the Buchwald–Hartwig Amination: Development, Applications, and Outlook

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