• English
    • Ελληνικά
    • Deutsch
    • français
    • italiano
    • español
  • français 
    • English
    • Ελληνικά
    • Deutsch
    • français
    • italiano
    • español
  • Ouvrir une session
Voir le document 
  •   Accueil de DSpace
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Voir le document
  •   Accueil de DSpace
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Voir le document
JavaScript is disabled for your browser. Some features of this site may not work without it.
Tout DSpace
  • Communautés & Collections
  • Par date de publication
  • Auteurs
  • Titres
  • Sujets

New short route to unsaturated fluoroketonucleosides: Case of 5-fluoro-1-(6-0-acetyl-3,4-di-deoxy-3-fluoro-β-D-glycero-hex-3-eno-pyranos- 2-ulosyl) uracil

Thumbnail
Auteur
Egron, M. J.; Komiotis, D.; Dorange, I.; Herscovici, J.; Ollapally, A. P.; Antonakis, K.
Date
2005
DOI
10.1081/NCN-59683
Sujet
5 fluoro 1 (6 o acetyl 3,4 dideoxy 3 fluoro beta dextro glycerohex 3 enopyranos 2 ulosyl)uracil
acetic acid derivative
fluorine derivative
hydroxyl group
ketone derivative
nucleoside derivative
unclassified drug
uracil derivative
acetylation
article
deprotection reaction
drug synthesis
elimination reaction
oxidation
reaction analysis
Chromatography, Thin Layer
Fluorine
Fluorouracil
Immunosuppressive Agents
Ketones
Magnetic Resonance Spectroscopy
Models, Chemical
Nucleosides
Uracil
Afficher la notice complète
Résumé
The proposed short synthesis involves two key steps: Oxidation of the isopropylidene derivative of the 3-fluoronucleoside possessing a free hydroxyl group in 2-position and acetylation of deprotected 3-fluoro-2-ketonucleoside which, after a β-elimination reaction, gives the desired unsaturated ketonucleoside 5. Copyright © Taylor & Francis, Inc.
URI
http://hdl.handle.net/11615/27295
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

Related items

Showing items related by title, author, creator and subject.

  • Thumbnail

    Multicomponent reaction of aldehydes, amines and oxalacetate analogues leading to biologically attractive pyrrole derivatives 

    Manta S., Kollatos N., Mitsos C., Chatzieffraimidi G.-A., Papanastasiou I., Gallos J.K., Komiotis D. (2020)
    Pyrrole is a very important pharmacophoric moiety. It has been widely incorporated into the skeleton of antitumor, anti-inflammatory, antibacterial, antioxidant and antifungal active substances. Access to this key heterocycle ...
  • Thumbnail

    Antiviral unsaturates nucleosides 

    Komiotis, D.; Manta, S.; Tsoukala, E.; Tzioumaki, N. (2008)
    In the search for effective, selective and nontoxic antiviral agents, a variety of nucleoside analogues have been synthesized, with different functionalities in the carbohydrate moiety. Unsaturated nucleoside analogues are ...
  • Thumbnail

    Acinetobacter baumannii antibiotic resistance mechanisms 

    Kyriakidis I., Vasileiou E., Pana Z.D., Tragiannidis A. (2021)
    Acinetobacter baumannii is a Gram-negative ESKAPE microorganism that poses a threat to public health by causing severe and invasive (mostly nosocomial) infections linked with high mortality rates. During the last years, ...
htmlmap 

 

Parcourir

Tout DSpaceCommunautés & CollectionsPar date de publicationAuteursTitresSujetsCette collectionPar date de publicationAuteursTitresSujets

Mon compte

Ouvrir une sessionS'inscrire
Help Contact
DepositionAboutHelpContactez-nous
Choose LanguageTout DSpace
EnglishΕλληνικά
htmlmap