Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mirna Balkadjian"'
Autor:
István Komáromi, Guido Zosimo-Landolfo, Alessandra Ricca, Françoise Barbalat-Rey, Gérald Bernardinelli, Mirna Balkadjian, Patrick Lichtle, Jean M. J. Tronchet, Michel Geoffroy
Publikováno v:
Journal of Carbohydrate Chemistry. 14:17-34
A series of 2,3-O-cyclopentylidene C-glycoside analogs in which the furanose ring has been replaced with a N-hydroxypyrrolidine have been prepared. A structural study of these tricyclic compounds and the aminoxyl radicals thereof has been carried out
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b252f3859df8aaa1b632e5412da8eb6
https://doi.org/10.1080/07328309508006434
https://doi.org/10.1080/07328309508006434
Autor:
A. Ricca, P. Lichtle, Martina Zsély, Françoise Barbalat-Rey, Guido Zosimo-Landolfo, Michel Geoffroy, Daniel Cabrini, Jean M. J. Tronchet, Mirna Balkadjian
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4118c604f9a02c4f8595b6b3f7582615
https://doi.org/10.1002/chin.199219302
https://doi.org/10.1002/chin.199219302
Autor:
Daniel Cabrini, Guido Zosimo-Landolfo, Mirna Balkadjian, Jean M. J. Tronchet, Fabienne Villedon-Denaide, Françoise Barbalat-Rey
Publikováno v:
ChemInform. 22
Cyclopentylidene ketals, moderately more acid-labile than their isopropylidene analogs, offer an alternative to the latter blocking groups. They have been shown to resist a large variety of reaction conditions commonly encountered in carbohydrate che
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e10f825c863936334040461b08d0da41
https://doi.org/10.1002/chin.199145275
https://doi.org/10.1002/chin.199145275
Autor:
Patrick Lichtle, Jean M. J. Tronchet, Alessandra Ricca, Guido Zosimo-Landolfo, Françoise Barbalat-Rey, Mirna Balkadjian, Daniel Cabrini, Martina Zsély, Michael Geoffroy
Publikováno v:
Tetrahedron Letters. 32:4129-4132
Analogs of blocked furanose ( 20 ) or pyranose sugars (i.e. 15 ) and of nucleosides (i.e. 23 ) in which the ring oxygen has been replaced with a -N(OH)-bridge have been prepared in generally good yields by a general reductive cyclization procedure pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::798ebd1c1dff7449b3cdbe73df71b90a
https://doi.org/10.1016/s0040-4039(00)79882-0
https://doi.org/10.1016/s0040-4039(00)79882-0
Autor:
Fabienne Villedon-Denaide, Mirna Balkadjian, Guido Zosimo-Landolfo, Françoise Barbalat-Rey, Jean M. J. Tronchet, Daniel Cabrini
Publikováno v:
Journal of Carbohydrate Chemistry. 9:823-835
Cyclopentylidene ketals, moderately more acid-labile than their isopropylidene analogs, offer an alternative to the latter blocking groups. They have been shown to resist a large variety of reaction conditions commonly encountered in carbohydrate che
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1eb492616c0bf81a256b26d78c553cd3
https://doi.org/10.1080/07328309008543877
https://doi.org/10.1080/07328309008543877