1994
DOI: 10.1039/p19940000153
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Fluorination of 5′-deoxy-5′-(methylthio)adenosine with xenon difluoride provides an expedient synthesis of (fluoromethylthio)adenosine

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Cited by 6 publications
(1 citation statement)
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“…A convenient method for the synthesis of 5 H -(fluoromethylthio)adenosine derivatives (242) (yield 70%) by regioselective fluorination of 5-methylthioadenosine derivatives 243 by XeF 2 has been proposed. 397 In this case, as in the fluorination of the 392 and biotin derivatives, 394 the reaction occurs at the least substituted carbon atom.…”
Section: Xef2mentioning
confidence: 99%
“…A convenient method for the synthesis of 5 H -(fluoromethylthio)adenosine derivatives (242) (yield 70%) by regioselective fluorination of 5-methylthioadenosine derivatives 243 by XeF 2 has been proposed. 397 In this case, as in the fluorination of the 392 and biotin derivatives, 394 the reaction occurs at the least substituted carbon atom.…”
Section: Xef2mentioning
confidence: 99%