Zobrazeno 1 - 10
of 155
pro vyhledávání: '"Jacques Defaye"'
Autor:
Nicolas Guilloteau, José M. García Fernández, Christophe Di Giorgio, Jacques Defaye, Pierre Vierling, Juan M. Benito, Alejandro Méndez-Ardoy, Céline Bienvenu, José L. Jiménez Blanco, Alejandro Díaz-Moscoso, Carmen Ortiz Mellet, Loïc Le Gourriérec
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
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Fully homogeneous facial amphiphiles consisting in a cyclodextrin (CD) platform onto which a polycationic cluster and a multi-tail hydrophobic moiety have been installed (polycationic amphiphilic CDs; paCDs) self-organized in the presence of plasmid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4160a8af24d9f3fb973cd396a9e1799
https://doi.org/10.1016/j.biomaterials.2011.06.025
https://doi.org/10.1016/j.biomaterials.2011.06.025
Publikováno v:
Annales Pharmaceutiques Françaises. 65:33-49
Resume Les proprietes de complexation des cyclomaltooligosaccharides (cyclodextrines, CDs), structures cage biocompatibles issues des biotechnologies, ont ete mises a profit dans les trente dernieres annees pour solubiliser, stabiliser et augmenter l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5201c92f9cf6f63c136181e4f17b0b1b
https://doi.org/10.1016/s0003-4509(07)90015-2
https://doi.org/10.1016/s0003-4509(07)90015-2
Autor:
Carmen Ortiz Mellet, Juan M. Benito, José M. García Fernández, Jacques Defaye, Paula Díaz-Pérez, M. Isabel García-Moreno
Publikováno v:
Carbohydrate Research. 337:2329-2334
Tandem Staudinger–aza-Wittig reaction of primary azidodeoxy sugars with triphenylphosphine–carbon disulfide affords the corresponding primary deoxyisothiocyanato sugars in high yield. No products arising from O→N acyl migration or formation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02ad682730fbbf0918a3b8b9f327e403
https://doi.org/10.1016/s0008-6215(02)00273-2
https://doi.org/10.1016/s0008-6215(02)00273-2
Autor:
Kazimierz Chmurski, Jacques Defaye
Publikováno v:
Supramolecular Chemistry. 12:221-224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ff1b9438b10c60d59e92f5689127f2c
https://doi.org/10.1080/10610270008027455
https://doi.org/10.1080/10610270008027455
Publikováno v:
European Journal of Organic Chemistry. 1999:1143-1152
The sulfur-linked pentathiohexasaccharide 3I,3IV-di-β-D-glucopyranosylthiogentiotetraose (12) has been prepared by a convergent approach involving the reaction of 1,2,4-tri-O-acetyl-6-deoxy-6-iodo-3-S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-3-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0984b5d6442ccebf267a866ca15eb404
https://doi.org/10.1002/(sici)1099-0690(199905)1999:5<1143::aid-ejoc1143>3.0.co
https://doi.org/10.1002/(sici)1099-0690(199905)1999:5<1143::aid-ejoc1143>3.0.co
Publikováno v:
The Journal of Organic Chemistry. 63:3572-3580
1‘-Thiotrehalulose (1-S-α-d-glucopyranosyl-1-thio-d-fructose, 6) and 1‘-epi-thiotrehalulose (1-S-β-d-glucopyranosyl-1-thio-d-fructose, 12) have been prepared, and their reactivity toward base and a...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c83139f47071b414eb490853341237d
https://doi.org/10.1021/jo972203k
https://doi.org/10.1021/jo972203k
Autor:
Jacques Defaye, France-Isabelle Auzanneau, Jacques Gelas, Danielle Promé, Khalil Bennis, Elisabeth Fanton
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :3629-3636
The synthesis of S-linked thio-analogues of chitobiose diversely substituted at both 2-acetamido-2-deoxy-D-glucopyranosyl units has been achieved successfully starting either from a 1,6-anhydro-4-O-triflyl galactosaminide derivative in reaction with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a455a48529c3ed56c9898e5cda2d19b
https://doi.org/10.1039/a802932f
https://doi.org/10.1039/a802932f
Autor:
Jacques Defaye, Kazimierz Chmurski
Publikováno v:
Tetrahedron Letters. 38:7365-7368
Per (6-bromo-6-deoxy)cyclomalto-hexaose, -heptaose, and -octaose and the corresponding per (6-chloro-6-deoxy) derivatives were prepared in high yield by reaction of bromomethylenemorpholinium bromide or chloromethylenemorpholinium chloride, respectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1ea117648967145f76d85ce24927a66
https://doi.org/10.1016/s0040-4039(97)10019-3
https://doi.org/10.1016/s0040-4039(97)10019-3
Publikováno v:
Journal of Inclusion Phenomena and Molecular Recognition in Chemistry. 29:57-63
The hemolytic properties of naturalcyclodextrins, especially of the more commoncyclomaltoheptaose entity, severely hamper theirpotential use as carriers in pharmaceuticalapplications where parenteral administration isconcerned. A systematic investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3efbf3917b390c44e741d1b472d3e986
https://doi.org/10.1023/a:1007919719275
https://doi.org/10.1023/a:1007919719275
Publikováno v:
Carbohydrate Research. 291:85-98
Reaction of a series of aminodeoxy-pentitols and -hexitols in anhydrous hydrogen fluoride with formic acid as catalyst gave the corresponding 2,5- and 3,6-anhydro-aminodeoxyalditols; namely, 1-amino-2,5-anhydro-1-deoxy-d-arabinitol, -d-xylitol, and -
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::826844f555c2f37aaafdc9c881e81298
https://doi.org/10.1016/s0008-6215(96)00164-4
https://doi.org/10.1016/s0008-6215(96)00164-4