Volume 58, Issue 11 pp. 3571-3574
Communication

Enantioconvergent Cross-Couplings of Alkyl Electrophiles: The Catalytic Asymmetric Synthesis of Organosilanes

Dr. Gregg M. Schwarzwalder

Dr. Gregg M. Schwarzwalder

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125 USA

These authors contributed equally to this work.

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Carson D. Matier

Carson D. Matier

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125 USA

These authors contributed equally to this work.

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Prof. Gregory C. Fu

Corresponding Author

Prof. Gregory C. Fu

Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125 USA

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First published: 16 January 2019
Citations: 69

Graphical Abstract

Enantioconvergent cross-couplings with electrophiles that lack a directing group or a proximal p/π orbital were achieved for the first time. Specifically, a chiral nickel catalyst can accomplish Negishi reactions of racemic α-halosilanes with alkylzinc reagents with good enantioselectivity under simple and mild conditions, thereby providing access to enantioenriched organosilanes, an important class of target molecules.

Abstract

Metal-catalyzed enantioconvergent cross-coupling reactions of alkyl electrophiles are emerging as a powerful tool in asymmetric synthesis. To date, high enantioselectivity has been limited to couplings of electrophiles that bear a directing group or a proximal p/π orbital. Herein, we demonstrate for the first time that enantioconvergent cross-couplings can be achieved with electrophiles that lack such features; specifically, we establish that a chiral nickel catalyst can accomplish Negishi reactions of racemic α-halosilanes with alkylzinc reagents with good enantioselectivity under simple and mild conditions, thereby providing access to enantioenriched organosilanes, an important class of target molecules.

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