Sequential Palladium‐Catalysed Direct Arylation Followed by Suzuki Coupling of Bromo‐2‐chloropyridines: Simple Access to a Variety of 2‐Arylpyridines-Reference-Cited by-同舟云学术

Sequential Palladium‐Catalysed Direct Arylation Followed by Suzuki Coupling of Bromo‐2‐chloropyridines: Simple Access to a Variety of 2‐Arylpyridines

Published:2012-08-24 Issue:28 Volume:2012 Page:4454-4462
ISSN:1434-1948
Container-title:European Journal of Inorganic Chemistry
language:en
Short-container-title:Eur. J. Inorg. Chem.

Author:

Baloch Marya¹,Roy David¹,Bensaid Souhila¹,Guerchais Véronique¹,Doucet Henri¹

Affiliation:

1. Institut Sciences Chimiques de Rennes, UMR 6226 CNRS – Université de Rennes 1, “Organométalliques: Matériaux et Catalyse”, Campus de Beaulieu, 35042 Rennes, France , Fax: +33‐2‐23236939, http://scienceschimiques.univ‐rennes1.fr/catalyse/personnels/interface/HD.htm

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejic.201200613

Reference83 articles.

1. For the use of 2‐arylpyridines substituted by heteroarenes in material chemistry see:

2. Vibrational spectroscopic characterization of rigid rod polymers: 3. Microstructural changes in stressed polymers

3. Enhanced electron injection and efficiency in blended-layer organic light emitting diodes with aluminium cathodes: new 2,5-diaryl-1,3,4-oxadiazole–fluorene hybrids incorporating pyridine units

4. A Supramolecularly-Caged Ionic Iridium(III) Complex Yielding Bright and Very Stable Solid-State Light-Emitting Electrochemical Cells

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