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- W2076187410 abstract "Ribosylzeatin tritiated on the purine ring with a specific activity of 829 × 1010 Bq (22 mCi) per millimole was easily prepared by allylic oxidation of N6-(Δ2-isopentenyl)[2,8-3H]adenosine which had been synthesized by alkylation of commercially available [2,8-3H]adenosine. This allylic oxidation gave mainly the trans-isomer which was obtained free of the cis-isomer and with a radiochemical purity of 99.8% by a one-step purification using reversed-phase HPLC. This simple procedure yields ribosylzeatin, the most common naturally occurring cytokinin, labelled with tritium at near maximum specific activity." @default.
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- W2076187410 date "1987-01-01" @default.
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- W2076187410 title "The synthesis of tritiated ribosylzeatin with high specific activity" @default.
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- W2076187410 doi "https://doi.org/10.1016/s0031-9422(00)82332-8" @default.
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