20201-56-3Relevant articles and documents
Synthesis of 8-(1,2,3-triazol-1-yl)-7-deazapurine nucleosides by azide–alkyne click reactions and direct C[sbnd]H bond functionalization
Kavoosi, Sam,Rayala, Ramanjaneyulu,Walsh, Brenna,Barrios, Maria,Gonzalez, Walter G.,Miksovska, Jaroslava,Mathivathanan, Logesh,Raptis, Raphael G.,Wnuk, Stanislaw F.
supporting information, p. 4364 - 4367 (2016/09/13)
Treatment of toyocamycin or sangivamycin with 1,3-dibromo-5,5-dimethylhydantoin in MeOH (rt/30?min) gave 8-bromotoyocamycin and 8-bromosangivamycin in good yields. Nucleophilic aromatic substitution of 8-bromotoyocamycin with sodium azide provided novel 8
Pyrrolopyrimidine nucleosides. 3. The total synthesis of toyocamycin, sangivamycin, tubercidin, and related derivatives.
Tolman,Robins,Townsend
, p. 2102 - 2108 (2007/10/04)
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