Synthesis, Antiviral, and Antimicrobial Evaluation of Benzyl Protected Diversified C -nucleosides
Formyl glycals are the versatile synthetic intermediates and can serves as precursor for the synthesis of various C and N-nucleosides. Due to the presence of electron donating and electron withdrawing character on formyl sugars which makes the molecule more susceptible to nucleophilic attack. Utiliz...
Saved in:
Published in | Frontiers in chemistry Vol. 6; p. 294 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
19.07.2018
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Formyl glycals are the versatile synthetic intermediates and can serves as precursor for the synthesis of various C and N-nucleosides. Due to the presence of electron donating and electron withdrawing character on formyl sugars which makes the molecule more susceptible to nucleophilic attack. Utilizing same strategy, we propose the synthesis of diversified
-nucleosides (
-
) by reaction with
,
dinucleophiles. These nucleoside analogs were than tested against viral, bacterial and fungal strains. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Christophe Len, University of Technology of Compiègne, France; Christophe Salome, SpiroChem AG, Switzerland This article was submitted to Medicinal and Pharmaceutical Chemistry, a section of the journal Frontiers in Chemistry Edited by: Laurent G. Désaubry, Université de Strasbourg, France |
ISSN: | 2296-2646 2296-2646 |
DOI: | 10.3389/fchem.2018.00294 |