1999
DOI: 10.1016/s0008-6215(99)00149-4
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Stereoselective synthesis of 3′-C-methylene- and 2′-methyl-3′-C-methylene-3′-deoxythymidine

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Cited by 2 publications
(1 citation statement)
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“…Likewise, compounds 52b,c and 52h were no inhibitory to virus replication at 200 or 400 g/mL. Riehokainen et al [80] have described the synthesis of 3 -C-methylene-(53a) and 2 -methyl-3 -C-methylene-3 -deoxythymidine (53b) (Fig. 27), without reporting any biological data.…”
Section: Exocyclic Methylene Nucleosidesmentioning
confidence: 99%
“…Likewise, compounds 52b,c and 52h were no inhibitory to virus replication at 200 or 400 g/mL. Riehokainen et al [80] have described the synthesis of 3 -C-methylene-(53a) and 2 -methyl-3 -C-methylene-3 -deoxythymidine (53b) (Fig. 27), without reporting any biological data.…”
Section: Exocyclic Methylene Nucleosidesmentioning
confidence: 99%