The Suzuki–Miyaura Cross‐Coupling as the Key Step in the Synthesis of 2‐Aminobiphenyls and 2,2'‐Diaminobiphenyls: Application in the Synthesis of Schiff Base Complexes of Zn-Reference-Cited by-同舟云学术

The Suzuki–Miyaura Cross‐Coupling as the Key Step in the Synthesis of 2‐Aminobiphenyls and 2,2'‐Diaminobiphenyls: Application in the Synthesis of Schiff Base Complexes of Zn

Published:2020-06-25 Issue:27 Volume:2020 Page:4208-4226
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Hylland Knut Tormodssønn¹^ORCID,Øien‐Ødegaard Sigurd¹^ORCID,Tilset Mats¹^ORCID

Affiliation:

1. Department of Chemistry University of Oslo P. O. Box 1033 Blindern 0315 Oslo Norway

Funder

Norges Forskningsråd

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202000599

Reference119 articles.

1. A Solution to the 2-Pyridyl Organometallic Cross-Coupling Problem: Regioselective Catalytic Direct Arylation of Pyridine N-Oxides

2. “Cationic” Suzuki–Miyaura Coupling with Acutely Base-Sensitive Boronic Acids

3. A General Solution for the 2-Pyridyl Problem

4. A General Solution for the 2-Pyridyl Problem

5. A New Palladium Precatalyst Allows for the Fast Suzuki−Miyaura Coupling Reactions of Unstable Polyfluorophenyl and 2-Heteroaryl Boronic Acids

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