Treatment of 8,2′-O-cycloadenosine (1a) and its benzoylation product with alkali gives 2′,3′-anhydro-8-oxyadenosine (2a) and its 6-N-benzoyl derivative (2b), respectively; under mildly alkaline conditions (2a) is converted back into (1a).
J. B. Chattopadhyaya and C. B. Reese, J. Chem. Soc., Chem. Commun., 1976, 860 DOI: 10.1039/C39760000860
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