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Versatile C(sp2)−C(sp3) Ligand Couplings of Sulfoxides for the Enantioselective Synthesis of Diarylalkanes

Dean, William M.; �iau?iulis, Mindaugas; Storr, Thomas E.; Lewis, William; Stockman, Robert A.

Authors

William M. Dean

Mindaugas �iau?iulis

Thomas E. Storr

William Lewis

Profile image of ROBERT STOCKMAN

ROBERT STOCKMAN robert.stockman@nottingham.ac.uk
Professor of Organic Chemistry



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.

Citation

Dean, W. M., Šiaučiulis, M., Storr, T. E., Lewis, W., & Stockman, R. A. (2016). Versatile C(sp2)−C(sp3) Ligand Couplings of Sulfoxides for the Enantioselective Synthesis of Diarylalkanes. Angewandte Chemie, 128(34), 10167-10170. https://doi.org/10.1002/ange.201602264

Journal Article Type Article
Acceptance Date Apr 29, 2016
Online Publication Date Jul 20, 2016
Publication Date Aug 16, 2016
Deposit Date Apr 21, 2021
Journal Angewandte Chemie
Print ISSN 0044-8249
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 128
Issue 34
Pages 10167-10170
DOI https://doi.org/10.1002/ange.201602264
Public URL https://nottingham-repository.worktribe.com/output/4869478
Publisher URL https://onlinelibrary.wiley.com/doi/abs/10.1002/ange.201602264