Hydrogenolysis of 3,5-0-benzylidene acet
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András Lipták; András Neszmélyi; Pavol Kováč; Ján Hirsch
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Article
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1981
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Elsevier Science
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French
⚖ 447 KB
Abebmt-The hydrogcnolysis of methyl 3,54benzylidene-a-and -/3-D-xylofuranoside derivatives with the LiAII&-AICI, reagent gave S-benzyl ethers as main products. In some cases the attack of the reagent occured at the ring oxygen of the furanoside skeleton to yield SObcnzyI-I-Omethylxylitol derivatives