William M. Dean
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
Mindaugas �iau?iulis
Thomas E. Storr
William Lewis
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 |
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