Synthesis and antiviral evaluation of 6'-substituted aristeromycins: potential mechanism-based inhibitors of S-adenosylhomocysteine hydrolase

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Abstract
New carbocyclic adenosine analogues substituted at the 6''-position with fluorine, hydroxyl, methylene, or hydroxymethyl have been synthesized as potential mechanism-based inhibitors of S-adenosylhomocysteine (AdoHcy) hydrolase. The synthetic routes began with a functionalized (.+-.)-azidocyclopentane 2, which was elaborated to the adenosine analogues, or with functionalized cyclopentane epoxides 11, 20, and 27, which were opened directly with adenine in the presence of base. The 6''.alpha.-fluoro (24), 6''.beta.-fluoro (10), and 6''-methylene (30) carbocylic adenosine analogues were potent inhibitors of AdoHcy hydrolase. None of the compounds displayed significant activity against herpes simplex virus type 1 to type 2, but several demonstrated potent inhibition of vaccinia virus replication.