Chemischer Informationsdienst
 1985
DOI: 10.1002/chin.198533340
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ChemInform Abstract: C‐NUCLEOSIDE STUDIES, PART 16. THE ISOPROPYLIDENATION OF D‐RIBOSE DIETHYL DITHIOACETAL AND RIBITOL. A NEW SYNTHESIS OF α‐ AND β‐D‐RIBOFURANOSYLETHYNE VIA 2,3:4,5‐DI‐O‐ISOPROPYLIDENE‐ALDEHYDO‐D‐RIBOSE

Gaffar Aslani-Shotorbani1,
J. G. Buchanan2,
Alan R. Edgar3
et al.

Abstract: Die Isopropylidenierung des Acetats (I) liefert die isomeren Diacetonide (II), die nach Deblockierung zu den Aldehydozuckem (III) in die Ribitole (IV) übergeführt werden.

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