Atropisomerism about Aryl–Csp3 Bonds: The Electronic and Steric Influence of ortho-Substituents on Conformational Exchange in Cannabidiol and Linderatin Derivatives-Reference-Cited by-同舟云学术

Atropisomerism about Aryl–Csp3 Bonds: The Electronic and Steric Influence of ortho-Substituents on Conformational Exchange in Cannabidiol and Linderatin Derivatives

Published:2014-06-23 Issue:13 Volume:79 Page:6015-6027
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Berber Hatice¹,Lameiras Pedro²,Denhez Clément¹³,Antheaume Cyril⁴,Clayden Jonathan⁵

Affiliation:

1. ICMR, CNRS UMR 7312, Faculté de Pharmacie, Université de Reims Champagne-Ardenne, 51 rue Cognacq-Jay, F-51096 Reims Cedex, France

2. ICMR, CNRS UMR 7312, Université de Reims Champagne-Ardenne, Moulin de la Housse, Bâtiment 18, BP 1039, F-51687 Reims Cedex 2, France

3. Multiscale Molecular Modeling Platform, Université de Reims Champagne-Ardenne, UFR Sciences Exactes et Naturelles, F-51687 Reims Cedex 2, France

4. Faculté de Pharmacie, Service Commun d’Analyse, 74 route du Rhin, BP 60024, F-67401 Illkirch Cedex, France

5. School of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo5006069

Reference45 articles.

1. Controlling Axial Conformation in 2-Arylpyridines and 1-Arylisoquinolines: Application to the Asymmetric Synthesis of QUINAP by Dynamic Thermodynamic Resolution

2. Dynamic Kinetic Resolution of Biaryl Atropisomers via Peptide-Catalyzed Asymmetric Bromination

3. Synthesis of Atropisomerically Defined, Highly Substituted Biaryl Scaffolds through Catalytic Enantioselective Bromination and Regioselective Cross-Coupling

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