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Chem.Res.Chin.Univ.2013,29(1),57—61
ANew toElvucitabine
Approach
Synthetic
ZHANG Yuan.yuanl,ZHAO Lin.shanlandCHENYan3
Ling.yul,LOU Gui.10n91,2+,ZHANG
and Institute Research,
,.TianjinKeyLaboratoryofMolecularDesignDrugDiscover.;,EanjinofPharmaceutical
R.CAina;
300193,P
Eanjin
2.School andPharmaceutical Institute,Jinan250353,尸足China
ofChemical Engineering,Shandong?olytechnic
Blood 25001R.China
Center,Jinan4,P
3.Shandong
AbstractAnew toelvucitabinestartedfrom viathereactionsof10 inanoverall
syntheticapproach L.xylose steps
of l
20%was included
yield developed.Thekeysteps trimethylsil3
stereocontrolled and choiceof I forthe of as
8-glycosidationexquisite chloroacetygroup protectionhydroxylgroups
wellasthe under mildcondition;.Thestructureofelvucitabine.in
correspondingdeprotectionnotably particular,the
was determined ofthe as1HNMR
stereochemistrythereoL properties.such
unambiguouslybycomparisonphysical
dataandthe rotation.ofthe withthose
specific synthesizedsample r‘-ported.
KeywordsElvucitabine;mntiviral;Nucleosidemethodology
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