Asymmetric Synthesis of Bicyclo[1.1.0]butyl, Azabicyclo[1.1.0]butyl, and Bicyclo[1.1.1]pentyl Sulfoximines using a SuFEx Reaction

03 June 2025, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

A sulfoxide-metal exchange reaction provides organometallic bicyclo[1.1.0]butyl, 1-azabicyclo[1.1.0]butyl, and bicyclo [1.1.1]pentyl reagents from the corresponding sulfoxides. Subsequent in situ SuFEx reactions with highly enantioenriched sulfonimidoyl fluoride precursors derived from (S)-N-(diisopropylcarbamoyl)-2-methylpropane-2-sulfonimidoyl fluoride (t-BuSF) allow for the asymmetric synthesis of novel bicyclo[1.1.0]butyl, 1-azabicyclo[1.1.0]butyl, and bicyclo[1.1.1]pentyl sulfoximines. These novel building blocks can be used for strain-release transformations and applications in medicinal chemistry.

Keywords

Bicyclo[1.1.0]butyl sulfoximines
1-Azabicyclo[1.1.0]butyl sulfoximines
Bicyclo[1.1.1]pentyl sulfoximines

Supplementary materials

Title
Description
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Title
Supplementary Materials for Asymmetric Synthesis of Bicyclo[1.1.0]butyl, Azabicyclo[1.1.0]butyl, and Bicyclo[1.1.1]pentyl Sulfoximines using a SuFEx Reaction
Description
Experimental protocols and spectral data
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