Diastereoselective Synthesis of N-tert-Butanesulfinylamines through Addition of p-Nitrobenzyl Chloride to N-tert-Butanesulfinimines Using a TDAE Strategy - Aix-Marseille Université Access content directly
Journal Articles SYNLETT Year : 2013

Diastereoselective Synthesis of N-tert-Butanesulfinylamines through Addition of p-Nitrobenzyl Chloride to N-tert-Butanesulfinimines Using a TDAE Strategy

Abstract

An easy and efficient method of diastereoselective synthesis of N-tert-butanesulfinylamines using a TDAE strategy was developed. Good yields and diastereoselectivities were achieved using readily available N-tert-butanesulfinimines and commercially available p-nitrobenzyl chloride.
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Dates and versions

hal-01425566 , version 1 (03-01-2017)

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Cédric Spitz, Omar Khoumeri, Thierry Terme, Patrice Vanelle. Diastereoselective Synthesis of N-tert-Butanesulfinylamines through Addition of p-Nitrobenzyl Chloride to N-tert-Butanesulfinimines Using a TDAE Strategy. SYNLETT, 2013, ⟨10.1055/s-0033-1339178⟩. ⟨hal-01425566⟩
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