Challenging nickel-catalysed amine arylations enabled by tailored ancillary ligand design-Reference-Cited by-同舟云学术

Challenging nickel-catalysed amine arylations enabled by tailored ancillary ligand design

Published:2016-03-23 Issue:1 Volume:7 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Lavoie Christopher M.,MacQueen Preston M.,Rotta-Loria Nicolas L.,Sawatzky Ryan S.,Borzenko Andrey,Chisholm Alicia J.,Hargreaves Breanna K. V.,McDonald Robert,Ferguson Michael J.,Stradiotto Mark

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms11073.pdf

Reference61 articles.

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3. Guram, A. S., Rennels, R. A. & Buchwald, S. L. A simple catalytic method for the conversion of aryl bromides to arylamines. Angew. Chem. Int. Ed. 34, 1348–1350 (1995).

4. Hartwig, J. F. Evolution of a fourth generation catalyst for the amination and thioetherification of aryl halides. Acc. Chem. Res. 41, 1534–1544 (2008).

5. Surry, D. S. & Buchwald, S. L. Biaryl phosphane ligands in palladium-catalyzed amination. Angew. Chem. Int. Ed. 47, 6338–6361 (2008).

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