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- W2046316124 abstract "Inosine was prepared (15% yield) by treatment of 5-amino-1-beta-D-ribofuranosyl-4-imidazolecarboxamide (AICA-riboside) with chloroform in the presence of sodium methoxide. This ring closure can be reasonably explained by assuming the formation of dichlorocarbene from chloroform and alkali. Carbon tetrachloride or hexachloroethane as a carbene source was more effective for the ring closure of AICA-riboside, giving inosine in 48% and 51% yields respectively." @default.
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- W2046316124 title "A new synthesis of inosine from 5-amino-l- -D-ribofuranosyl-4-imidazole-carboxamide" @default.
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- W2046316124 doi "https://doi.org/10.1093/nar/3.1.231" @default.
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