Rapid Synthesis of 3,3′ Bis-Arylated BINOL Derivatives Using a C–H Borylation in Situ Suzuki–Miyaura Coupling Sequence
Author:
Affiliation:
1. Department of Chemistry, 1-014 Center for Science and Technology, Syracuse University, Syracuse, New York 13244, United States
Funder
Syracuse University
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol502126r
Reference79 articles.
1. aRousseaux, S.; Liégault, B.; Fagnou, K.Modern Tools for the Synthesis of Complex Bioactive Molecules;John Wiley & Sons, Inc.: 2012; pp1–32.
2. Organic Chemistry in Drug Discovery
3. A General Method for the Enantioselective Synthesis of α-Chiral Heterocycles
4. Enantioselective Addition of Boronates to o-Quinone Methides Catalyzed by Chiral Biphenols
5. Asymmetric Methallylation of Ketones Catalyzed by a Highly Active Organocatalyst 3,3′-F2-BINOL
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