7‐Substituted 7‐Deaza‐2′‐deoxyguanosines: Regioselective Halogenation of Pyrrolo2,3‐dpyrimidine Nucleosides

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Structure of the archaeal transfer RNA nucleoside G*-15 (2-amino-4,7-dihydro- 4-oxo-7-beta-D-ribofuranosyl-1H-pyrrolo[2,3-d]pyrimidine-5-carboximi dam ide (archaeosine))1993 · 111 citations
2. 2Synthesis of 2-amino-7-(2'-deoxy-.beta.-D-erythro-pentofuranosyl)-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one, a new isostere of 2'-deoxyguanosine1983 · 94 citations
3. 3A dideazatetrahydrofolate analog lacking a chiral center at C-6: N-[4-[2-(2-amino-3,4-dihydro-4-oxo-7H-pyrrolo[2,3-d]pyrimidin-5yl)ethyl[benzoyl]-L-glutamic acid is an inhibitor of thymidylate synthase1992 · 254 citations
4. 4Cadeguomycin, a novel nucleoside analog antibiotic. II. Improved purification, physicochemical properties and structure assignment.1982 · 36 citations
5. 5Solid-phase synthesis of the self-complementary hexamer d(c7GpCpc7GpCpc7GpC) via the O-3′-phosphoramidite of 7-deaza-2′-deoxyguanosine1985 · 44 citations