Jump to main content
Jump to site search

Issue 6, 1998
Previous Article Next Article

Highly enantioselective synthesis of dialkyl and alkyl aryl N-tosylsulfimides

Abstract

Enantiomerically pure S-alkyl-S-[(4S)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]-N-tosylsulfimides react with Grignard reagents affording dialkyl and alkyl aryl sulfimides in high chemical yield and enantiomeric excess.

Back to tab navigation

Article type: Paper
DOI: 10.1039/A708977E
Citation: Chem. Commun., 1998,0, 701-702
  •   Request permissions

    Highly enantioselective synthesis of dialkyl and alkyl aryl N-tosylsulfimides

    G. Celentano and S. Colonna, Chem. Commun., 1998, 0, 701
    DOI: 10.1039/A708977E

Search articles by author

Spotlight

Advertisements