Zobrazeno 1 - 6
of 6
pro vyhledávání: '"M. Idriss Bennani-Baiti"'
Autor:
M. Idriss Bennani-Baiti, Françoise Leclercq, Kostas Antonakis, Charles Frayssinet, Marie-José Egron
Publikováno v:
Carbohydrate Research. 228:95-102
The title compound 5 was synthesized by direct oxidation of the fluoro precursor and not from an epoxyketo intermediate according to the Paulsen procedure, which has been used until now to obtain bromo- and chloro-ketonucleosides. Antineoplastic acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ac4ef45799a6fc55e63c417ce0cf1f0
https://doi.org/10.1016/s0008-6215(00)90551-2
https://doi.org/10.1016/s0008-6215(00)90551-2
Autor:
M. Idriss Bennani-Baiti, Jean Hersovici, Kostas Antonakis, Charles Frayssinet, Roland Montserret
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 1:721-724
Keto C-glycoside-fatty acid conjugates were synthesized from 6-hydroxy 2- and 4-keto unsaturated D-C-glycosides. These compounds were tested for cytotoxic activity against LFCl 2 A cells (Rat hepatocarcinoma cells). The introduction of a lipid chain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccf3baf9940b631848525803e0c8fa48
https://doi.org/10.1016/s0960-894x(01)81055-6
https://doi.org/10.1016/s0960-894x(01)81055-6
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 1:395-398
A series of 4-keto unsaturated C-glycosided was synthesized from O-acetyl C-glycosides. These compounds and some parent 2-keto unsaturated C-glycosides were tested for cytotoxic activity against LFCl 2 A cells (Rat hepatocarcinoma cells). C-Glycoside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9aee40767cd914b2f9222049631586d4
https://doi.org/10.1016/s0960-894x(00)80263-2
https://doi.org/10.1016/s0960-894x(00)80263-2
Autor:
M. Idriss Bennani-Baiti, Françoise Leclercq, Kostas Antonakis, Marie-José Ergon, Charles Frayssinet
Publikováno v:
Carbohydrate research. 248
Three fluoroketonucleosides ( 6 , 8 , and 11 ) have been synthesized by direct oxidation of the fluoro precursors. The presence of the highly electronegative fluorine atom in the α position to the carbonyl group favours hydration leading to the gem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef66d50cc87a1a3cc468f4bb2c3f7f97
https://pubmed.ncbi.nlm.nih.gov/8252530
https://pubmed.ncbi.nlm.nih.gov/8252530
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