Stereoselective synthesis of artificial C-nucleosides
Reported herein is a conceptually new synthetic route to 1’-aryl C-ribofuranosides and their 2’,3’-didehydro 2’,3’-dideoxy (D4) analogues. We have successfully implemented a divergent synthetic route capable to reach two important, biologically significant groups of compounds. The first two strategi...
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University of Glasgow
2008
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.518883 |