dc.creator | Egron, M. J. | en |
dc.creator | Komiotis, D. | en |
dc.creator | Dorange, I. | en |
dc.creator | Herscovici, J. | en |
dc.creator | Ollapally, A. P. | en |
dc.creator | Antonakis, K. | en |
dc.date.accessioned | 2015-11-23T10:26:05Z | |
dc.date.available | 2015-11-23T10:26:05Z | |
dc.date.issued | 2005 | |
dc.identifier | 10.1081/ncn-200059683 | |
dc.identifier.issn | 1525-7770 | |
dc.identifier.uri | http://hdl.handle.net/11615/27294 | |
dc.description.abstract | 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 beta-elimination reaction, gives the desired unsaturated ketonucleoside 5. | en |
dc.source.uri | <Go to ISI>://WOS:000230392700002 | |
dc.subject | BIOLOGICAL-ACTIVITY | en |
dc.subject | DERIVATIVES | en |
dc.subject | AGENT | en |
dc.subject | Biochemistry & Molecular Biology | en |
dc.title | New short route to unsaturated fluoroketonucleosides: Case of 5-fluoro-1-(6-O-acetyl-3,4-di-deoxy-3-fluoro-beta-D-glycero-hex-3-eno-py ranos-2-ulosyl) uracil | en |
dc.type | journalArticle | en |