Enantioselective Redox-Neutral Coupling of Aldehydes and Alkenes by an Iron-Catalyzed “Catch–Release” Tethering Approach
Author:
Affiliation:
1. Institute of Organic Chemistry, University of Vienna, Währinger Strasse 38, 1090 Vienna, Austria
Funder
Austrian Academy of Sciences
Universität Wien
H2020 European Research Council
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
http://pubs.acs.org/doi/pdf/10.1021/jacs.8b12242
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1. Metal-catalyzed reductive coupling of olefin-derived nucleophiles: Reinventing carbonyl addition
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3. Formation of C–C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation
4. Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon
5. Reductive Generation of Enolates from Enones Using Elemental Hydrogen: Catalytic C−C Bond Formation under Hydrogenative Conditions
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