Guy Solladié, Ph.D

Affiliations: 
Université Louis Pasteur, Strasbourg 
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"Guy Solladié"
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Publications

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Bauder C, Biard JF, Solladié G. (2006) Synthesis of derivatives of potent antitumor bistramides D and A leading to the first crystal structure of natural bistramide D. Organic & Biomolecular Chemistry. 4: 1860-2
Bonini C, Chiummiento L, Videtta V, et al. (2006) A concise and efficient stereoselective synthesis of the C1-C11 fragment of macrolactin A Synlett. 2427-2430
Colobert F, Obringer M, Solladié G. (2006) A new access to enantiopure syn- and anti-2-methyl-1,3-diol moieties from chiral nonracemic α-bromo α′-sulfinyl ketones promoted by samarium diiodide European Journal of Organic Chemistry. 1455-1467
Khiri N, Lefranc A, Solladié G, et al. (2005) Preparation of enantiomerically pure (E)-β-sulfinylenones from β-ketoesters Tetrahedron Letters. 46: 5807-5810
Lanners S, Khiri N, Solladié G, et al. (2005) Ring-opening of lactones with enolate nucleophiles: A simple access to functionalised β-ketoesters, β,δ-diketoesters and β-ketosulfoxides Tetrahedron Letters. 46: 619-622
Izzo I, Crumbie R, Solladié G, et al. (2005) Enantioselective sulfoxide-directed preparation of 1,2-diols from oxalic compounds: Formal synthesis of the 10-membered lactone core of ascidiatrienolides and didemnilactones Tetrahedron Asymmetry. 16: 1503-1511
Holzwarth R, Bartsch R, Cherkaoui Z, et al. (2005) New 2,2′-substituted 6,6′-dimethylbiphenyl derivatives inducing strong helical twisting power in liquid crystals European Journal of Organic Chemistry. 3536-3541
Holzwarth R, Bartsch R, Cherkaoui Z, et al. (2004) New 2,2′-substituted 4,4′-dimethoxy-6,6′-dimethyl[1, 1′-biphenyls], inducing a strong helical twisting power in liquid crystals Chemistry - a European Journal. 10: 3931-3935
Bonini C, Chiummiento L, Pullez M, et al. (2004) Convergent highly stereoselective preparation of the C12-C24 fragment of macrolactin A Journal of Organic Chemistry. 69: 5015-5022
Carreño MC, Sanz-Cuesta MJ, Colobert F, et al. (2004) Synthesis and trimethylaluminum additions on γ-hydroxy-δ- sulfinyl and sulfonyl enoates Organic Letters. 6: 3537-3540
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