Versatile C(sp2)−C(sp3) ligand couplings of sulfoxides for the enantioselective synthesis of diarylalkanes

Dean, William M., Šiaučiulis, Mindaugas, Storr, Thomas E., Lewis, William and Stockman, Robert A. (2016) Versatile C(sp2)−C(sp3) ligand couplings of sulfoxides for the enantioselective synthesis of diarylalkanes. Angewandte Chemie-International Edition, 55 (34). pp. 10013-10016. ISSN 1433-7851

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Abstract

The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomerically pure diarylalkanes in up to 98 % yield and greater than 99.5 % enantiomeric excess. This ligand coupling reaction is tolerant to multiple substitution patterns and provides access to diverse areas of chemical space in three operationally simple steps from commercially available reagents. This strategy provides orthogonal access to electron-deficient heteroaromatic compounds, which are traditionally synthesized by transition metal catalyzed cross-couplings, and circumvents common issues associated with proto-demetalation and β-hydride elimination.

Item Type: Article
Uncontrolled Keywords: arenes,cross-coupling,magnesium,reaction mechanisms,sulfur
Faculty \ School: Faculty of Science > School of Chemistry
UEA Research Groups: Faculty of Science > Research Groups > Chemistry of Materials and Catalysis
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Depositing User: Pure Connector
Date Deposited: 04 Mar 2017 01:41
Last Modified: 05 May 2024 01:14
URI: https://ueaeprints.uea.ac.uk/id/eprint/62849
DOI: 10.1002/anie.201602264

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