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Results: 1-3 |
Results: 3
Highly stereoselective route to dialkyl sulfoxides based upon the sequential displacement of oxygen and carbon leaving groups by Grignard reagents onsulfinyl compounds
Authors: Capozzi, MAM Cardellicchio, C Naso, F Spina, G Tortorella, P
Citation: Mam. Capozzi et al., Highly stereoselective route to dialkyl sulfoxides based upon the sequential displacement of oxygen and carbon leaving groups by Grignard reagents onsulfinyl compounds, J ORG CHEM, 66(17), 2001, pp. 5933-5936
Substituted benzene anions as leaving groups in the reaction of sulfinyl derivatives with grignard reagents: A new and convenient route to dialkyl sulfoxides in high enantiomeric purity
Authors: Capozzi, MAM Cardellicchio, C Naso, F Tortorella, P
Citation: Mam. Capozzi et al., Substituted benzene anions as leaving groups in the reaction of sulfinyl derivatives with grignard reagents: A new and convenient route to dialkyl sulfoxides in high enantiomeric purity, J ORG CHEM, 65(9), 2000, pp. 2843-2846
Enantioselective catalytic oxidation of (arylthio)- or (alkylthio)methylphosphonates as a route to enantiomeric pure aryl alkyl or dialkyl sulfoxides
Authors: Capozzi, MAM Cardellicchio, C Fracchiolla, G Naso, F Tortorella, P
Citation: Mam. Capozzi et al., Enantioselective catalytic oxidation of (arylthio)- or (alkylthio)methylphosphonates as a route to enantiomeric pure aryl alkyl or dialkyl sulfoxides, J AM CHEM S, 121(19), 1999, pp. 4708-4709
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