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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

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.

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext