A synthetic route to carbocyclic aminonucleosides

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Abstract

The carbocyclic aminonucleosides I (R = R2 = H, R1 = OH, R3 = H, Me; R = H, R1 = OH, R2 = 4-MeOC6H4CH2CH(NH2)CO, R3 = Me; R = OH, R1 = R2 = R3 = H) were prepd. from 2-azabicyclo[2.2.1]hept-5-en-3-one (II) via the pyrimidine III. [on SciFinder(R)]

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Daluge, S., & Vince, R. (1976). A synthetic route to carbocyclic aminonucleosides. Tetrahedron Letters, 17(35), 3005–3008. https://doi.org/10.1016/0040-4039(76)80055-X

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