Zobrazeno 1 - 10 of 12 pro vyhledávání: '"Paloma P. Méndez-Castrillón"'
1
Uridine-5′-Diphosphate Glucose Analogues. 21. Nucleoside Modified Analogues of Antiviral 5′-O-[[[[(α-D-Glucopyranosyl)Oxy Carbonyl]Amino]Sulfonyl]Uridine Derivatives
Autor: Federico G. De las Heras, Ma Teresa García-López, Piedad Fernández-Resa, Paloma P. Méndez-Castrillón, Ma José Camarasa
Publikováno v: Nucleosides and Nucleotides. 5:413-421
A series of uridine modified analogues of antiviral 5′-O-[[[[(α-D-glucopyranosyl) oxy] carbonyl]amno]sulfonyl]uridine derivatives has been synthesized by reaction of suitably protected glucose and glucosamine derivatives with CISO2-N=C=O and thymi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2aac4ea076614a9fe02f22000a001fa2
https://doi.org/10.1080/07328318608068682
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2
Synthesis of 2-(β-D-Ribofuranosyl)Thiazole-4-Carboxamide 5′-Phosphate Isosteres
Autor: J. Ignacio Andrés, Paloma P. Méndez-Castrillón, Federico G. De las Heras, Ma Teresa García-López
Publikováno v: Nucleosides and Nucleotides. 5:423-429
SUMMARY. The syntheses of 5′-O-sulfamoyl and 5′-O-carbamoyl tiazofurin (9 and 12) are described. One pot reaction of 2′, 3′-O-isopropylidene-tiazofurin (7) with hexabutyldistannoxane and sulfamoyl chloride gave the corresponding 5′-O-sulfam
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::08044c65daabe75ba58f826c08a819a0
https://doi.org/10.1080/07328318608068683
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3
Hexose-modified anti-viral analogues of uridine 5′-disphosphate glucose derivatives
Autor: Ana San Félix, Jose M. Fiandor, Paloma P. Méndez-Castrillón, Balbino Alarcón, Luis Carrasco, Federico G. De las Heras, M.-T. Garcia-Lopez
Publikováno v: European Journal of Medicinal Chemistry. 22:59-65
A series of analogues of the anti-viral 5′- O -[[[[(tetrabenzyl-, or tetrabenzoyl-α- d -glucopyranosyl)oxy]-carbonyl]amino]sulfonyl]uridine, in which the α-glucose moiety has been replaced by α-mannose, or galactose, 2-acetamido-2-deoxy-α-gluco
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6081e88c24895b6c4784a3cfed88bf6a
https://doi.org/10.1016/0223-5234(87)90174-7
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4
Synthesis and Cytostatic Activity of Halomethylthiazole C-Nucleosides and Analogues1
Autor: M. Teresa García-López, Rosario Herranz, Paloma P. Méndez-Castrillón
Publikováno v: Nucleosides and Nucleotides. 1:127-138
The synthesis of 2-(β-D-ribofuranosyl)-and 2-(tetrahydropyran-2-yl)-4-halomethylthiazoles from 2, 5-anhydro-D-allonthioamide and tetrahydropyran-2-thiocarboxamide is described. Bromination of 2-(β-D-ribofuranosyl)- and 2-tetrahydropyran-2-yl)-4-met
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fb774883eb7382c2c401f080e3c934f4
https://doi.org/10.1080/07328318208078827
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6
Synthesis and Antiviral Activity of 5′-O-Sulfamoyluridine Derivatives
Autor: S. Perez, Carmen Gil-Fernández, Angel García Gancedo, Jose M. Fiandor, María Teresa García-López, Paloma P. Méndez-Castrillón, Pilar Vilas, Concepción Pérez, Federico G. De las Heras
Publikováno v: Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
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A series of 5′-O-[[[[(alkyl)oxy]carbonyl] amino] sulfonyl] uridines have been synthesized by reaction of cyclohexanol, palmityl alcohol, 1,2-di-O-benzoylpropanetriol and 2,3,4,6-tetra-O-benzoyl-L-glucopyranose with chlorosulfonyl isocyanate and 2,3
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d97e9615eb983030d081303cd0400400
https://doi.org/10.1080/07328318908054171
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