N-oxides of adenosine-type nucleosides undergo pyrimidine ring opening and closure to give 5-amino-4-(1,2,4-oxadiazol-3-yl)imidazole derivatives
Treatment of acylated adenosine N-oxides with carboxylic anhydrides and thiophenol resulted in pyrimidine ring opening followed by exocyclic ring closure. Ammonolysis gave 5-amino-4-(5-substituted-1,2,4-oxadiazol-3-yl)-1- (β-D-ribofuranosyl)imidazole deri
Nowak, Ireneusz,Cannon, John F.,Robins, Morris J.
p. 4565 - 4568
(2007/10/03)
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Get Best Price for913626-75-2Acetic acid (2R,3S,5R)-2-acetoxymethyl-5-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)-5-phenylsulfanylmethyleneamino-imidazol-1-yl]-tetrahydro-furan-3-yl ester