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Results: 1-19 |
Results: 19
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
Asymmetric synthesis of beta-hydroxyesters by aldol type condensation of enantiomerically pure t-butyl p-tolyl sulfinyl acetate: unexpected substituent effect on the absolute configuration of the product
Authors: Solladie, G Bauder, C Arce-Dubois, E Pasturel-Jacope, Y
Citation: G. Solladie et al., Asymmetric synthesis of beta-hydroxyesters by aldol type condensation of enantiomerically pure t-butyl p-tolyl sulfinyl acetate: unexpected substituent effect on the absolute configuration of the product, TETRAHEDR L, 42(15), 2001, pp. 2923-2925
Correlation between molecular structure and helicity of induced chiral nematics in terms of short-range and electrostatic-induction interactions. Thecase of chiral biphenyls
Authors: di Matteo, A Todd, SM Gottarelli, G Solladie, G Williams, VE Lemieux, RP Ferrarini, A Spada, GP
Citation: A. Di Matteo et al., Correlation between molecular structure and helicity of induced chiral nematics in terms of short-range and electrostatic-induction interactions. Thecase of chiral biphenyls, J AM CHEM S, 123(32), 2001, pp. 7842-7851
Enantioselective synthesis of the unsymmetrical bis(lactone) (-)-(3E,6R,9E,12S,14R)-colletol induced by chiral sulfoxides and an approach to (+)-colletodiol by asymmetric hydroxylation of an alpha,beta-hydroxy lactone
Authors: Solladie, G Gressot, L Colobert, F
Citation: G. Solladie et al., Enantioselective synthesis of the unsymmetrical bis(lactone) (-)-(3E,6R,9E,12S,14R)-colletol induced by chiral sulfoxides and an approach to (+)-colletodiol by asymmetric hydroxylation of an alpha,beta-hydroxy lactone, EUR J ORG C, (2), 2000, pp. 357-364
Hemisynthesis of bistramide D by stereoselective reduction of bistramide A. Partial determination of relative and absolute configurations
Authors: Solladie, G Bauder, C Biard, JF
Citation: G. Solladie et al., Hemisynthesis of bistramide D by stereoselective reduction of bistramide A. Partial determination of relative and absolute configurations, TETRAHEDR L, 41(40), 2000, pp. 7747-7750
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
Highly stereoselective synthesis of enantiomerically pure B-hydroxy-gamma-sulfenyl-gamma-butyrolactone by asymmetric Pummerer type cyclization
Authors: Solladie, G Wilb, N Bauder, C
Citation: G. Solladie et al., Highly stereoselective synthesis of enantiomerically pure B-hydroxy-gamma-sulfenyl-gamma-butyrolactone by asymmetric Pummerer type cyclization, TETRAHEDR L, 41(21), 2000, pp. 4189-4192
Stereoselective synthesis of all-trans methyl substituted polyenes by reductive elimination and application to the synthesis of all-trans 3-methyl-nona-2,4,6-trienol
Authors: Solladie, G Colobert, F Kalai, C
Citation: G. Solladie et al., Stereoselective synthesis of all-trans methyl substituted polyenes by reductive elimination and application to the synthesis of all-trans 3-methyl-nona-2,4,6-trienol, TETRAHEDR L, 41(21), 2000, pp. 4197-4200
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
Biomimetic synthesis of the flavanone leridol, revision of the structure of the natural product
Authors: Solladie, G Gehrold, N Maignan, J
Citation: G. Solladie et al., Biomimetic synthesis of the flavanone leridol, revision of the structure of the natural product, EUR J ORG C, (9), 1999, pp. 2309-2314
A chiral beta,delta-dioxo-epsilon-sulfinyl ester in a convergent enantioselective synthesis towards the C-1-C-13 polyol fragment of amphotericin B
Authors: Solladie, G Wilb, N Bauder, C
Citation: G. Solladie et al., A chiral beta,delta-dioxo-epsilon-sulfinyl ester in a convergent enantioselective synthesis towards the C-1-C-13 polyol fragment of amphotericin B, EUR J ORG C, (11), 1999, pp. 3021-3026
Applications of chiral sulfoxides in enantioselective synthesis of diols and total synthesis of natural products
Authors: Solladie, G
Citation: G. Solladie, Applications of chiral sulfoxides in enantioselective synthesis of diols and total synthesis of natural products, ENANTIOMER, 4(3-4), 1999, pp. 183-193
Synthesis of (+)-(R)-5-hydroxy-6-hydroxymethyl-7-methoxy-8-methylflavanone
Authors: Solladie, G Gehrold, N Maignan, J
Citation: G. Solladie et al., Synthesis of (+)-(R)-5-hydroxy-6-hydroxymethyl-7-methoxy-8-methylflavanone, TETRAHEDR-A, 10(14), 1999, pp. 2739-2747
1,4 Asymmetric Induction in the carbonyl reduction of a gamma-ketosulfoxide.
Authors: Solladie, G Colobert, F Somny, F
Citation: G. Solladie et al., 1,4 Asymmetric Induction in the carbonyl reduction of a gamma-ketosulfoxide., TETRAHEDR L, 40(6), 1999, pp. 1227-1228
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
First stereocontrolled synthesis of the (3S,5R,7R,10R,11R)-C1-C13 fragmentof nystatin A(1)
Authors: Solladie, G Wilb, N Bauder, C Bonini, C Viggiani, L Chiummiento, L
Citation: G. Solladie et al., First stereocontrolled synthesis of the (3S,5R,7R,10R,11R)-C1-C13 fragmentof nystatin A(1), J ORG CHEM, 64(15), 1999, pp. 5447-5452
Enantioselective approach to polyhydroxylated compounds using chiral sulfoxides: Synthesis of enantiomerically pure myo-inositol and pyrrolidine derivatives
Authors: Colobert, F Tito, A Khiar, N Denni, D Medina, MA Martin-Lomas, M Ruano, JLG Solladie, G
Citation: F. Colobert et al., Enantioselective approach to polyhydroxylated compounds using chiral sulfoxides: Synthesis of enantiomerically pure myo-inositol and pyrrolidine derivatives, J ORG CHEM, 63(24), 1998, pp. 8918-8921
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