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Results: 1-7 |
Results: 7
Synthesis of menthyl sulfinate and sulfoxides on solid phase
Authors: Rolland, C Hanquet, G Ducep, JB Solladie, G
Citation: C. Rolland et al., Synthesis of menthyl sulfinate and sulfoxides on solid phase, TETRAHEDR L, 42(51), 2001, pp. 9077-9080
Wang p-alkoxyphenylsulfoxide as a new linker and Pummerer cleavage strategy in solid-phase preparation of 1,2-diols
Authors: Rolland, C Hanquet, G Ducep, JB Solladie, G
Citation: C. Rolland et al., Wang p-alkoxyphenylsulfoxide as a new linker and Pummerer cleavage strategy in solid-phase preparation of 1,2-diols, TETRAHEDR L, 42(43), 2001, pp. 7563-7566
Regio- and diastereoselection in the oxaziridinium salt oxidation of acyclic allylic acetates
Authors: Poisson, D Cure, C Solladie, C Hanquet, G
Citation: D. Poisson et al., Regio- and diastereoselection in the oxaziridinium salt oxidation of acyclic allylic acetates, TETRAHEDR L, 42(22), 2001, pp. 3745-3748
Stereoselective synthesis towards the C8-C18 subunit of pamamycin-607 induced by a chiral sulfoxide group
Authors: Solladie, G Salom-Roig, XJ Hanquet, G
Citation: G. Solladie et al., Stereoselective synthesis towards the C8-C18 subunit of pamamycin-607 induced by a chiral sulfoxide group, TETRAHEDR L, 41(4), 2000, pp. 551-554
Diastereodivergent synthesis of the C8-C18 precursor and C1 '-C11 ' subunit of pamamycin 607 induced by a chiral sulfoxide group
Authors: Solladie, G Salom-Roig, XJ Hanquet, G
Citation: G. Solladie et al., Diastereodivergent synthesis of the C8-C18 precursor and C1 '-C11 ' subunit of pamamycin 607 induced by a chiral sulfoxide group, TETRAHEDR L, 41(15), 2000, pp. 2737-2740
Asymmetric synthesis of syn and anti 1,2-diols from diethyl oxalate using the stereoselective sulfoxide directed reduction of 1,2-diketone derivatives
Authors: Solladie, G Hanquet, G Izzo, I Crumbie, R
Citation: G. Solladie et al., Asymmetric synthesis of syn and anti 1,2-diols from diethyl oxalate using the stereoselective sulfoxide directed reduction of 1,2-diketone derivatives, TETRAHEDR L, 40(15), 1999, pp. 3071-3074
Stereoselective sulfoxide directed reduction of 1,2-diketo-derivatives to enantiomerically pure syn and anti 1,2-diols. Correction of the relative configuration by X-ray and chemical correlation to goniobutenolides A and B.
Authors: Solladie, G Hanquet, G Rolland, C
Citation: G. Solladie et al., Stereoselective sulfoxide directed reduction of 1,2-diketo-derivatives to enantiomerically pure syn and anti 1,2-diols. Correction of the relative configuration by X-ray and chemical correlation to goniobutenolides A and B., TETRAHEDR L, 40(1), 1999, pp. 177-180
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