In-depth structure–selectivity investigations on asymmetric, copper-catalyzed oxidative biaryl coupling in the presence of 5-cis-substituted prolinamines
Author:
Affiliation:
1. Organic Chemistry Laboratory
2. University of Bayreuth
3. 95447 Bayreuth
4. Germany
5. Institute of Organic Chemistry
6. University of Würzburg
7. 97074 Würzburg
Abstract
Copper complexes of 5-cis-substituted prolinamines provided up to 87% ee in the enantioselective oxidative biaryl coupling of 3-hydroxy-2-naphthoates.
Funder
Deutsche Forschungsgemeinschaft
Publisher
Royal Society of Chemistry (RSC)
Subject
Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2015/CY/C4CY01676A
Reference117 articles.
1. Natural Bridged Biaryls with Axial Chirality and Antimitotic Properties
2. The Biocatalytic Repertoire of Natural Biaryl Formation
3. 1,1‘-Binaphthyl Dimers, Oligomers, and Polymers: Molecular Recognition, Asymmetric Catalysis, and New Materials
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