Nucleosides CXI. 6,6′-Anhydro-hexofurano
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Brian A. Otter; Elvira A. Falco
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Article
📅
1978
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Elsevier Science
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French
⚖ 269 KB
Recent studies from this laboratory have shown that 6,5'-cyclopyrlmidine nucleosides2, for example the isopropylideneuridine analogue 1, are very susceptible to oxidation at C-5'. Thus, autoxidation3 of 1. with 02-NaOH, or treatment with Mn02 in methanol readily affords the 5'-ketonucleoside 4. The