Benzoyl Groups as ortho -Substituents in Cannabidiol Derivatives: Controlling Axial Conformation about Aryl-C(sp3 ) Bonds
Author:
Affiliation:
1. ICMR; UMR CNRS 7312; Université de Reims Champagne-Ardenne; 51 rue Cognacq-Jay 51096 Reims Cedex France
2. ICMR; UMR CNRS 7312; Université de Reims Champagne-Ardenne; Moulin de la Housse, Bâtiment 18, BP 1039 51687 Reims Cedex 2 France
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201800340/fullpdf
Reference32 articles.
1. Atroposelective Synthesis of Axially Chiral Biaryl Compounds
2. Atropselektive Synthese axial-chiraler Biaryle
3. Nonbiaryl and Heterobiaryl Atropisomers: Molecular Templates with Promise for Atropselective Chemical Transformations
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1. Atropisomerism about aryl–C(sp3) bonds: chemically driven rotational pathway in cannabidiol derivatives;Organic & Biomolecular Chemistry;2023
2. Cajanusoids A–D, Unusual Atropisomeric Stilbene Dimers with PTP1B Inhibitory Activities from the Leaves of Cajanus cajan;The Journal of Organic Chemistry;2021-04-08
3. Synthetic Strategies for (−)‐Cannabidiol and Its Structural Analogs;Chemistry – An Asian Journal;2019-10-08
4. Intramolecular OH/π versus C–H/O H-Bond-Dependent Conformational Control about Aryl–C(sp3) Bonds in Cannabidiol Derivatives;Organic Letters;2019-08-20
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