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- W1979290424 abstract "Starting from a readily available enantiopure building block, a straightforward enantioselective approach to 3′-methyl-2′,3′-β-oxirane-fused carbanucleosides bearing adenosine analogues is detailed. The key steps in the syntheses involved a lipase-catalyzed regioselective monoacylation of a diol to obtain the key intermediate and direct coupling of this key intermediate with diversely substituted purine nucleobases under Mitsunobu reaction conditions providing only the N9 target molecules." @default.
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- W1979290424 date "2007-06-01" @default.
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- W1979290424 title "Chemoenzymatic synthesis of novel adenosine carbanucleoside analogues containing a locked 3′-methyl-2′,3′-β-oxirane-fused system" @default.
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- W1979290424 doi "https://doi.org/10.1016/j.tet.2007.03.122" @default.
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