Asymmetric Synthesis of <i>S</i> -Trifluoromethyl Sulfoxide and Sulfoximine Pharmacophores

-acyl group is first cleaved to give the free-NH sulfilimine that then undergoes hydrolysis by backside displacement of the amine to give the sulfoxide with inversion of stereochemistry.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-04-27
DOI
https://doi.org/10.1021/jacs.6c03062
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Asymmetric Synthesis of S -Trifluoromethyl Sulfoxide and Sulfoximine Pharmacophores

Jonathan A. Ellman, Justin Ye, Na Yeon Kwon
Journal of the American Chemical Society
Synthesis and Catalytic Reactions
article

Asymmetric Synthesis of S -Trifluoromethyl Sulfoxide and Sulfoximine Pharmacophores

Jonathan A. Ellman, Justin Ye, Na Yeon Kwon
article en

Abstract

-acyl group is first cleaved to give the free-NH sulfilimine that then undergoes hydrolysis by backside displacement of the amine to give the sulfoxide with inversion of stereochemistry.

Journal of the American Chemical SocietyVol. 148(17)
Yale University (US)
National Institute of General Medical Sciences
Openalex Percentile: Top 20%
Synthesis and Catalytic Reactions
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