Sergio Castillon
0000-0002-0690-7549
179 papers found
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New dithiolate-bridged rhodium complexes
Erratum: Stereoselective synthesis of nucleosides by metallocene-promoted activation of glycosyl fluorides (Tetrahedron Letters, 1992, 33, 1093)
Asymmetric hydroformylation of styrene by rhodium(I) catalysts with chiral ligands containing sulfur donors
Regioselective hydroformylation of cyclic vinyl and allyl ethers with rhodium catalysts. Crucial influence of the size of the phosphorus cocatalyst
A new and extremely fast synthesis of 2-deoxy-2,2-difluoro-d-arabino-hexose (2-deoxy-2,2-difluoro-d-glucose)
Hydroformylation of glucal derivatives with rhodium catalysts. Crucial influence of the auxiliary ligand tris(ortho-tert-butylphenyl) phosphite
Catalytic hydroformylation of alkenes with cationic dinuclear rhodium(I) complexes, and the effect of the couter ions
gem-difluorination versus 1,2-migration and fragmentation in the reaction of 2- and 3-uloses with DAST. Influence of stereochemistry at the anomeric carbon atom
Low-pressure selective hydroformylation of 2,3- and 2,5-dihydrofuran with a rhodium catalyst. Unexpected influence of the auxiliary ligand tris(o-t-butylphenyl) phosphite
A route to functionalized branched-chain amino sugars via nitrous acid promoted spiroaziridine formation
Synthesis of methyl 3-acetamido-4-O-benzoyl-2,3,6-trideoxy-2-fluoro-β-l-mannopyranoside: a protected 2-fluoro analogue of acosamine
Chiral synthons for the total synthesis of fluoro amino acids and fluoro analogues of antibiotic sugars
Synthesis of benzyl and methyl 3-benzamido-2,3,6-trideoxy-2-fluoro-β-l-galactopyranoside: Protected C-2 fluoro analogues of daunosamine
Synthesis of 2′-C-fluoro-β-daunomycin. An example of configurational retention in fluorodehydroxylation with diethylaminosulfur trifluoride
Hydroxy group directed hydrogenation with rhodium and iridium catalysts. Synthesis of a protected chiral carbocyclic analogue of daunosamine
Oxygen-17 NMR and oxygen-18-induced isotopic shifts in carbon-13 NMR for the elucidation of a controversial reaction mechanism in carbohydrate chemistry
Diazo-, azo-, and azidoazoles. VII. Imidazo[1,2-b]-versusimidazo[2,1-c]benzo-as-triazines
200-MHz proton nuclear magnetic resonance study of the naphtho[2,1-e]tetrazolo[5,1-c]-as-triazine/3-azidonaphtho[2,1-e]-as -triazine/naphtho[2,1-e]tetrazolo[1,5-b-]-as-triazine equilibrium
Effect of substituents on the 3-azidobenzo-as-triazine/tetrazolo[5,1-c]benzo-as-triazine/tetrazolo[1,5-b] benzo-as-triazine equilibrium
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