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Results: 1-10 |
Results: 10
Capillary electrophoretic resolution of chiral aryl alkyl and aryl benzyl sulphoxides using sulphated beta-cyclodextrins as chiral selectors
Authors: Hadley, MR Decrette, M Guillore, G Rosini, C Donnoli, MI Superchi, S Hutt, AJ
Citation: Mr. Hadley et al., Capillary electrophoretic resolution of chiral aryl alkyl and aryl benzyl sulphoxides using sulphated beta-cyclodextrins as chiral selectors, J SEP SCI, 24(9), 2001, pp. 766-776
Towards a correlation of absolute configuration and chiroptical propertiesof alkyl aryl sulfoxides: A coupled-oscillator foundation of the empiricalMislow rule?
Authors: Rosini, C Donnoli, MI Superchi, S
Citation: C. Rosini et al., Towards a correlation of absolute configuration and chiroptical propertiesof alkyl aryl sulfoxides: A coupled-oscillator foundation of the empiricalMislow rule?, CHEM-EUR J, 7(1), 2001, pp. 72-79
Synthesis and stereochemical characterization of optically active 1,2-diarylethane-1,2-diols: Useful chiral controllers in the Ti-mediated enantioselective sulfoxidation
Authors: Donnoli, MI Scafato, P Superchi, S Rosini, C
Citation: Mi. Donnoli et al., Synthesis and stereochemical characterization of optically active 1,2-diarylethane-1,2-diols: Useful chiral controllers in the Ti-mediated enantioselective sulfoxidation, CHIRALITY, 13(5), 2001, pp. 258-265
New ligands for manganese catalysed selective oxidation of sulfides to sulfoxides with hydrogen peroxide
Authors: Brinksma, J La Crois, R Feringa, BL Donnoli, MI Rosini, C
Citation: J. Brinksma et al., New ligands for manganese catalysed selective oxidation of sulfides to sulfoxides with hydrogen peroxide, TETRAHEDR L, 42(24), 2001, pp. 4049-4052
Determination of absolute configuration using vibrational circular dichroism spectroscopy: The chiral sulfoxide 1-(2-methylnaphthyl) methyl sulfoxide
Authors: Stephens, PJ Aamouche, A Devlin, FJ Superchi, S Donnoli, MI Rosini, C
Citation: Pj. Stephens et al., Determination of absolute configuration using vibrational circular dichroism spectroscopy: The chiral sulfoxide 1-(2-methylnaphthyl) methyl sulfoxide, J ORG CHEM, 66(11), 2001, pp. 3671-3677
Chromatographic resolution and elution order of alkyl aryl and aryl benzylsulfoxides on cellulose-based chiral stationary phases
Authors: Donnoli, MI Superchi, S Rosini, C
Citation: Mi. Donnoli et al., Chromatographic resolution and elution order of alkyl aryl and aryl benzylsulfoxides on cellulose-based chiral stationary phases, ENANTIOMER, 5(2), 2000, pp. 181-188
Determination of the absolute configuration of 1-arylethane-1,2-diols by anonempirical analysis of the CD spectra of their 4-biphenylboronates
Authors: Superchi, S Donnoli, MI Rosini, C
Citation: S. Superchi et al., Determination of the absolute configuration of 1-arylethane-1,2-diols by anonempirical analysis of the CD spectra of their 4-biphenylboronates, ORG LETT, 1(13), 1999, pp. 2093-2096
Enantiopure 1,2-diarylethane-1,2-diols as chiral auxiliaries in stereoselective processes: Induction of molecular and supramolecular chirality
Authors: Rosini, C Superchi, S Donnoli, MI
Citation: C. Rosini et al., Enantiopure 1,2-diarylethane-1,2-diols as chiral auxiliaries in stereoselective processes: Induction of molecular and supramolecular chirality, ENANTIOMER, 4(1), 1999, pp. 3-23
Induction of cholesteric mesophases by simple cyclic derivatives of p,p '-disubstituted 1,2-diphenylethane-1,2-diols: Importance of shape and polarizability effects
Authors: Superchi, S Donnoli, MI Proni, G Spada, GP Rosini, C
Citation: S. Superchi et al., Induction of cholesteric mesophases by simple cyclic derivatives of p,p '-disubstituted 1,2-diphenylethane-1,2-diols: Importance of shape and polarizability effects, J ORG CHEM, 64(13), 1999, pp. 4762-4767
Catalytic asymmetric oxidation of aryl sulfides with a Ti/H2O/(R,R)-diphenylethane-1,2-diol complex: a versatile and highly enantioselective oxidation protocol
Authors: Donnoli, MI Superchi, S Rosini, C
Citation: Mi. Donnoli et al., Catalytic asymmetric oxidation of aryl sulfides with a Ti/H2O/(R,R)-diphenylethane-1,2-diol complex: a versatile and highly enantioselective oxidation protocol, J ORG CHEM, 63(25), 1998, pp. 9392-9395
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