Copper–Hydride-Catalyzed Enantioselective Processes with Allenyl Boronates. Mechanistic Nuances, Scope, and Utility in Target-Oriented Synthesis
Author:
Affiliation:
1. Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, United States
2. Supramolecular Science and Engineering Institute, University of Strasbourg, CNRS, 67000 Strasbourg, France
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.9b05465
Reference56 articles.
1. Recent progress in copper-catalyzed difunctionalization of unactivated carboncarbon multiple bonds
2. Copper-catalyzed borylative transformations of non-polar carbon–carbon unsaturated compounds employing borylcopper as an active catalyst species
3. Cu-Catalyzed Borylative and Silylative Transformations of Allenes: Use of β-Functionalized Allyl Copper Intermediates in Organic Synthesis
4. Cu‐Catalyzed Chemoselective Preparation of 2‐(Pinacolato)boron‐Substituted Allylcopper Complexes and their In Situ Site‐, Diastereo‐, and Enantioselective Additions to Aldehydes and Ketones
5. Catalytic diastereo- and enantioselective additions of versatile allyl groups to N–H ketimines
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