56039-11-3Relevant articles and documents
LITHIATION OF AN IMIDAZOLE NUCLEOSIDE AT THE C-5 POSITION. SYNTHESIS OF 3-DEAZAGUANOSINE FROM URIDINE
Tanaka, Hiromichi,Hirayama, Masashi,Matsuda, Akira,Miyasaka, Tadashi,Ueda, Tohru
, p. 589 - 592 (1985)
3-Deazaguanosine, an antiviral nucleoside, was synthesized from uridine via lithiation of a C-2 protected imidazole nucleoside, which has been devised as a method for introducing various functionalities to the C-5 position.This furnished the first success
Nucleosides and Nucleotides. 116. Convenient Syntheses of 3-Deazaadenosine, 3-Deazaguanosine, and 3-Deazainosine via Ring Closure of 5-Ethynyl-1-β-D-ribofuranosylimidazole-4-carboxamide or -carbonitrile
Minakawa, Noriaki,Matsuda, Akira
, p. 557 - 570 (2007/10/02)
An easy chemical synthesis of 3-deazapurine nucleosides, 3-deazainosine pyridin-4(5H)-one (8)>, 3-deazaguanosine pyridin-4(5H)-one (23)>, and 3-deazaadenosine 4-amino-1-β-D-ribof
A Lithiation route to C-5 substitution of an imidazole nucleoside and its application to the synthesis of 3-deazaguanosine
Tanaka,Hirayama,Suzuki,Miyasaka
, p. 1971 - 1980 (2007/10/02)
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