Role of the Base in Buchwald–Hartwig Amination-Reference-Cited by-同舟云学术

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Role of the Base in Buchwald–Hartwig Amination

Published:2014-11-04 Issue:24 Volume:79 Page:11961-11969
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Sunesson Ylva¹,Limé Elaine²,Nilsson Lill Sten O.²,Meadows Rebecca E.³,Norrby Per-Ola¹²

Affiliation:

1. Department of Chemistry and Molecular Biology, University of Gothenburg, Kemigården 4, SE-412 96 Göteborg, Sweden

2. Pharmaceutical Development, Global Medicines Development, AstraZeneca, Pepparedsleden 1, SE-431 83 Mölndal, Sweden

3. Pharmaceutical Development, AstraZeneca, Silk Road Business Park, Macclesfield SK10 2NA, United Kingdom

Funder

European Commission

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo501817m

Reference51 articles.

1. Carbon−Heteroatom Bond-Forming Reductive Eliminations of Amines, Ethers, and Sulfides

2. Carbon–heteroatom bond formation catalysed by organometallic complexes

3. Dialkylbiaryl phosphines in Pd-catalyzed amination: a user's guide

4. A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines

5. Palladium-catalyzed synthesis of arylamines from aryl halides. Mechanistic studies lead to coupling in the absence of tin reagents

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