Direct Orthoruthenation of Planar Prochiral Pyridine Derivatives by C−H Bond Activation with [Ru(CO)2Cl2]n and Its Unexpected Stereoselectivity-Reference-Cited by-同舟云学术

Direct Orthoruthenation of Planar Prochiral Pyridine Derivatives by C−H Bond Activation with [Ru(CO)2Cl2]n and Its Unexpected Stereoselectivity

Published:2006-05-12 Issue:12 Volume:45 Page:4589-4591
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Hijazi Akram¹,Djukic Jean-Pierre¹,Pfeffer Michel¹,Ricard Louis¹,Kyritsakas-Gruber Nathalie¹,Raya Jesus¹,Bertani Philippe¹,de Cian André¹

Affiliation:

1. Institut de Chimie de Strasbourg, CNRS LC3 UMR 7177, and Laboratoire de Chimie de Coordination Organique, CNRS UMR 7140, Université Louis Pasteur, 4 rue Blaise Pascal, 67000 Strasbourg, France, and Laboratoire de Chimie des Hétéro-éléments et de Coordination, CNRS UMR 7653, Ecole Polytechnique, 91128 Palaiseau Cedex, France

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic0604112

Reference24 articles.

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3. Regioselective palladation of 2-oxazolinyl-[2.2]paracyclophanes.

4. Catalytic Asymmetric Rearrangement of Allylic N-Aryl Trifluoroacetimidates. A Useful Method for Transforming Prochiral Allylic Alcohols to Chiral Allylic Amines

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