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Application of the Oxo Reaction to a 3,4-Ene

When 3-deoxy-l,2 5,6-di-0-isopropylidene-a-D-erythro-hex-3-en-ose (63) was allowed to react with carbon monoxide and hydrogen in the presence of preformed dicobalt octacarbonyl, the reaction [Pg.100]

Application of the Oxo Reaction to 5,6-DlDEOXY-l,2-0-ISOPROPYLIDENE-a-D- ylo-HEX-5-ENOFURANOSE [Pg.101]

T reatment of 5,6-dideoxy- l,2-0-isopropylidene-a -D-zi/Zo-hex-5-eno-furanose (65) with carbon monoxide and hydrogen in the presence [Pg.101]

Acetylation of the mixture of products from the oxo reaction on the 3-acetate of (65) afforded a mixture of compounds that was shown, by gas — liquid chromatography, to consist of three main components in about 90% yield. Further work is in progress on the determination of the structure of the remaining components. [Pg.102]


See other pages where Application of the Oxo Reaction to a 3,4-Ene is mentioned: [Pg.59]    [Pg.100]   


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