Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 20, 1983
Previous Article Next Article

An enantiomerically pure α-sulphinyl-N,N-dimethylacetamide: a new, efficient reagent for enantioselective aldol-type condensation

Abstract

Asymmetric synthesis (up to 99%) of β-hydroxy-N,N-dimethylacetamides was achieved starting from aldehydes and an optically active sulphoxide containing synthon, the sense of chiral discrimination depending on the intermediate metal enolate.

Back to tab navigation

Article information


J. Chem. Soc., Chem. Commun., 1983, 1138-1139
Article type
Paper

An enantiomerically pure α-sulphinyl-N,N-dimethylacetamide: a new, efficient reagent for enantioselective aldol-type condensation

R. Annunziata, M. Cinquini, F. Cozzi, F. Montanari and A. Restelli, J. Chem. Soc., Chem. Commun., 1983, 1138
DOI: 10.1039/C39830001138

Search articles by author

Spotlight

Advertisements