Issue 12, 1977

Reaction of 8,2′-O-cycloadenosine with hydrazine and amines. Convenient preparations of 9-β-D-arabinofuranosyladenine and its derivatives

Abstract

Reaction between 8,2′-O-cycloadenosine (2) and hydrazine gives a high yield of (1b) which on oxidation with yellow mercuric oxide is converted into ara-A (1a) in quantitative yield; reaction between (2) and the appropriate amines gives the 8-amino-ara-A derivatives (1cg) in good to high yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 414-415

Reaction of 8,2′-O-cycloadenosine with hydrazine and amines. Convenient preparations of 9-β-D-arabinofuranosyladenine and its derivatives

J. B. Chattopadhyaya and C. B. Reese, J. Chem. Soc., Chem. Commun., 1977, 414 DOI: 10.1039/C39770000414

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