A new practical one-pot access to sulfonimidates

Organic Letters

Volumn 4, Issue 23, 2002, Pages 4093-4095

  Leca, Dominique ^a   Fensterbank, Louis ^a   Lacôte, Emmanuel ^a   Malacria, Max ^a  

^a CNRS   (France)

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ARTICLE;

EID: 0041736678     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol026837b     Document Type: Article

References (23)

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21. a values of the two intermediates have not been measured, but there is usually a four-unit gap between sulfonyl and sulfinyl derivatives.
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23. Our initial experiments show that chirality on the sulfur is destroyed during the reaction. Enantiopure sulfinamides lead to racemic sulfonimidates. Transfer of chirality from auxiliaries on nitrogen is under study.