Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Pastora Borrachero"'
Publikováno v:
Proceedings of The 20th International Electronic Conference on Synthetic Organic Chemistry.
Adenoviruses (Ads) are common pathogens in patients with compromised immunity being a potentially life-threatening disease. Human Ads are usually associated with respiratory infections, gastroenteritis or viral conjunctivitis among others pathologies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5d183fc4a93f0e92ba5e29cc1012765
https://doi.org/10.3390/ecsoc-20-a011
https://doi.org/10.3390/ecsoc-20-a011
Synthesis of fluorescent O-Coumarin glycosides as Potential drug delivery systems for MAO inhibitors
Autor:
Óscar López, Francisca Cabrera-Escribano, Antonio Franconetti, José G. Fernández-Bolaños, Pastora Borrachero
Publikováno v:
Proceedings of The 19th International Electronic Conference on Synthetic Organic Chemistry.
Nowadays, the high prevalence and incidence of neurodegenerative diseases, such as Parkinson, Alzheimer or amyotrophic lateral sclerosis diseases makes an important field to search for novel molecules to access different customized treatment. In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3b7fb419f1157568119f63c7bed080c
https://doi.org/10.3390/ecsoc-19-a024
https://doi.org/10.3390/ecsoc-19-a024
Autor:
Manuel Gómez-Guillén, Simeón Pérez-Garrido, Francisca Cabrera-Escribano, M. D. Estrada, Manuel Angulo-Álvarez, Pastora Borrachero, Ma Jesús Diánez, Ma Isabel Torres-Sánchez, Amparo López-Castro
Publikováno v:
Tetrahedron: Asymmetry. 16:3897-3907
A short and efficient route to enantiomerically pure hexahydroxy- and pentahydroxy-perhydroazaazulenes, ring-homologues of castanospermine, starting from the sole isoxazolidine derivative obtained in the 1,3-dipolar cycloaddition of a d -galactose-de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f09853e9488edb89f2bd8c4492862c7f
https://doi.org/10.1016/j.tetasy.2005.10.023
https://doi.org/10.1016/j.tetasy.2005.10.023
Publikováno v:
Tetrahedron: Asymmetry. 16:889-897
Ready access to constrained, multifunctionalized, hydrolytically stable amino acids has been established by the synthesis of their direct precursors using 2,5-anhydro-3-azido-3-deoxy- d -altrose (a ‘formyl azido- C -glycofuranoside’), or its read
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7eef7d1b4e19c9dc1eb333e451e8b00d
https://doi.org/10.1016/j.tetasy.2004.12.024
https://doi.org/10.1016/j.tetasy.2004.12.024
Publikováno v:
Tetrahedron Letters. 45:4835-4839
Regio- and stereoselective cycloaddition of methyl acrylate to C-glycosyl nitrones derived from d -galactose and d -glucose, giving 5-methoxycarbonyl-3-(pentoglycos-5-yl or pentitol-1-yl)isoxazolidines, is reported. Transformation of one of them into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b1fc41e9f42e4f11cc3de7f102ede8f
https://doi.org/10.1016/j.tetlet.2004.04.161
https://doi.org/10.1016/j.tetlet.2004.04.161
Autor:
Yolanda Vera-Ayoso, Ana T. Carmona, Francisca Cabrera-Escribano, Pastora Borrachero, Manuel Gómez-Guillén
Publikováno v:
Tetrahedron: Asymmetry. 15:429-444
Reaction of diversely configured and substituted, unbranched methyl d -hexopyranosides with the DAST in dichloromethane or acetonitrile led to normal substitution products and/or rearranged fluoro compounds (ring-contracted 2,5-anhydro-1-fluoro-1- O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9a12f6e681f56584eef26b0c9e201b4
https://doi.org/10.1016/j.tetasy.2003.11.034
https://doi.org/10.1016/j.tetasy.2003.11.034
Autor:
Ma Isabel Torres, Francisca Cabrera-Escribano, Amparo López Castro, Simeón Pérez-Garrido, Pastora Borrachero, Ma Jesús Diánez, Manuel Gómez-Guillén, M. D. Estrada
Publikováno v:
Tetrahedron: Asymmetry. 13:2025-2038
Protected C7 and C8 aminodialdoses were prepared stereoselectively from readily available C5 and C6 monosaccharide N-benzyl nitrones, by regio- and diastereoselective 1,3-dipolar cycloaddition reactions with vinyl trimethylsilane, followed by acetyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4535a03945a05f7eb539c1e950e1f060
https://doi.org/10.1016/s0957-4166(02)00543-8
https://doi.org/10.1016/s0957-4166(02)00543-8
Autor:
M. D. Estrada, Francisca Cabrera-Escribano, Yolanda Vera-Ayoso, Manuel Gómez-Guillén, Pastora Borrachero, Simeón Pérez-Garrido, Amparo López-Castro, Ma Jesús Diánez
Publikováno v:
Tetrahedron: Asymmetry. 12:2031-2041
Novel, potentially bioactive, fluorinated branched-chain monosaccharides were obtained by reaction of diethylaminosulphur trifluoride (DAST) with a series of methyl 3-C-cyano-3-ethoxycarbonyl-β- d -glucopyranoside derivatives, including the 4,6-O-be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6f406c12e591a98c7c1f85a905e277f
https://doi.org/10.1016/s0957-4166(01)00354-8
https://doi.org/10.1016/s0957-4166(01)00354-8
Publikováno v:
Tetrahedron: Asymmetry. 11:2927-2946
Fluorination of diverse 3-deoxy-3- C -methyl-3-nitro-hexopyranosides and hexo-1-thiopyranosides of the d - and l -series by the DAST reagent was studied in order to establish, on this 3-branched-chain sugar domain, the influence of the stereochemical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::403447fa40c4fdff427237d9d685047a
https://doi.org/10.1016/s0957-4166(00)00252-4
https://doi.org/10.1016/s0957-4166(00)00252-4
Autor:
Pastora Borrachero, Manuel Gómez-Guillén, Francisca Cabrera-Escribano, Rafael Ojeda, Ana T. Carmona, Ma Jesús Diánez, Amparo López-Castro, M. D. Estrada, Simeón Pérez-Garrido
Publikováno v:
Tetrahedron: Asymmetry. 10:1751-1764
Mixed crystals of methyl 3-deoxy-3- C -methyl-3-nitro-α- d - and β- l -glucopyranosides (1:1), easily available from d -glucose by means of the Baer reaction, were completely characterised by X-ray diffraction analysis. These diastereomeric compone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ba36edf6e63ab715834f66b72fd73d5
https://doi.org/10.1016/s0957-4166(99)00156-1
https://doi.org/10.1016/s0957-4166(99)00156-1