Stereocontrolled synthesis of (5+5), (5+6) and (6+6) 3-spiropseudonucleosides von Gasch, Consolación, Illangua, José M., Merino-Montiel, Penélope, Fuentes, José

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The use of anhydroiminocyclitols as glycosyl donors in glycosidation reactions von Fuentes, José, Al Bujuq, Nader R., Angulo, Manuel, Gasch, Consolación

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Spiranic d- gluco-configured N-substituted thiohydantoins as potential enzymatic inhibitors von Gasch, Consolación, Merino-Montiel, Penélope, López, Óscar, Fernández-Bolaños, José G., Fuentes, José

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Simple and efficient conversion of N,N-dimethylhydrazones and aldehydes to nitriles von Fernández, Rosario, Gasch, Consolacíon, Lassaletta, Jose-María, Llera, José-Manuel, Vázquez, Juan

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Iminosugar thioglycosides as glycosyl donors: a route to disaccharides with an iminosugar moiety von Fuentes, José, Al Bujuq, Nader R., Angulo, Manuel, Gasch, Consolación

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Stereocontrolled synthesis of iminocyclitols with an ether bridge von Sayago, Francisco J., Fuentes, José, Angulo, Manuel, Gasch, Consolación, Ángeles Pradera, M.

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Isothiocyanatoulosonates, a new type of glycosyl isothiocyanate useful for the stereocontrolled synthesis of thiohydantoin spironucleosides von Gasch, Consolación, Salameh, Bader A.B, Pradera, M.Angeles, Fuentes, José

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Corrigendum to “Stereocontrolled synthesis of (5+5), (5+6) and (6+6) 3-spiropseudonucleosides” [Tetrahedron 65 (21) (2009) 4149–4155] von Gasch, Consolación, Illangua, José M., Merino-Montiel, Penélope, Fuentes, José

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Stereocontrolled synthesis of thiohydantoin spironucleosides from sugar spiroacetals von Fuentes, José, Salameh, Bader A.B., Angeles Pradera, M., Fernández de Córdoba, Francisco J., Gasch, Consolación

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Expeditious synthesis of sulfoazetidine spiro- C-glycosides from ketose acetals von Sayago, Francisco J., Ángeles Pradera, M., Gasch, Consolación, Fuentes, José

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Highly efficient nitroaldol reaction promoted by trialkylsilyl chlorides von Fernández, Rosario, Gasch, Consolación, Gómez-Sánchez, Antonio, Vilchez, José Eduardo

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An easy route to seven-membered iminocyclitols from aldohexopyranosyl enamines von Fuentes, José, Gasch, Consolación, Olano, David, Pradera, M.Ángeles, Repetto, Guillermo, Sayago, Francisco J.

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Isothiocyanato derivatives of sugars in the stereoselective synthesis of spironucleosides and spiro- C-glycosides von Gasch, Consolación, Pradera, M.Angeles, Salameh, Bader A.B., Molina, José L., Fuentes, José

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d-Ribofuranosylenamine: a versatile starting material for preparing azasugar thioglycosides and building blocks for thioureylene-di-nucleosides von Fuentes, José, Illangua, José M., Sayago, Francisco J., Angulo, Manuel, Gasch, Consolación, Pradera, M. Ángeles

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Anhydroazasugars as key intermediates in the stereocontrolled preparation of azasugars and their ethyl thioglycosides von Fuentes, José, Sayago, Francisco J., Illangua, José M., Gasch, Consolación, Angulo, Manuel, Ángeles Pradera, M.

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Stereoselective synthesis of azasugar thioglycosides von Pradera, M.Angeles, Sayago, Francisco J., Illangua, José M., Gasch, Consolación, Fuentes, José

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Ring contraction of glycopyranosyl enamines: an easy route to furanoid thioglycosides of 5-aminosugars von Pradera, M.Ángeles, Sayago, Francisco J., Illangua, José M., Angulo, Manuel, Gasch, Consolación, Fuentes, José

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Formaldehyde SAMP-Hydrazone as a Neutral Chiral Formyl Anion and Cyanide Equivalent: Asymmetric Michael Additions to Nitroalkenes von Enders, Dieter, Syrig, Ralf, Raabe, Gerhard, Fernández, Rosario, Gasch, Consolación, Lassaletta, José-María, Llera, José-Manuel

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Chiral thioxohydroimidazoles with two sugar moieties. N-, C-, and spiro-nucleosides von Gasch, Consolación, Pradera, M.Angeles, Salameh, Bader A.B, Molina, José L, Fuentes, José

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Formaldehyde dimethylhydrazone: A new neutral reagent for nucleophilic hydroformylation and hydrocyanation von Lassaletta, José-María, Fernández, Rosario, Gasch, Consolación, Vázquez, Juan

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