Synthesis of 8-Substituted Analogues of 2′-Deoxy-2′-Fluoroadenosine

T Maruyama, S Kozai, T Manabe, Y Yazima…

Index: Maruyama; Utsumi; Sato; Richman Nucleosides and Nucleotides, 1994 , vol. 13, # 6-7 p. 1219 - 1230

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Citation Number: 4

Abstract

Abstract After 3′, 5′-di-O-protection of 8-bromoadenosine, the product was converted to the arabinoside, which was successively treated with diethylaminosulfur trifluoride (DAST) and acid to afford 8-bromo-2′-deoxy-2′-fluoroadenosine. However, the formation of an 8,