Synthesis of C-5'-nor-dideoxycarbanucleosides structurally related to neplanocin C.

M J Comin, C A Pujol, E B Damonte, J B Rodriguez
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引用次数: 7

Abstract

Purine carbanucleosides built on a 6-oxabicyclo[3.1.0]hexane template were synthesized from readily available 2-cyclopentenone employing a Mitsunobu reaction to incorporate the base onto the carbocyclic ring. Both adenosine and guanosine analogues exhibited moderate antiviral activity.

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与新菌素结构相关的C-5′-非二脱氧碳核苷的合成。
以2-环戊烯酮为原料,采用Mitsunobu反应将碱结合到碳环上,合成了基于6-氧杂环[3.1.0]己烷模板的嘌呤碳核苷。腺苷和鸟苷类似物均表现出中等的抗病毒活性。
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