Abstract
Pressure hydrogenation using Raney nickel or ruthenium on charcoal, of secondary and tertiary γ-furylalkanols is described. The products are the corresponding homologs of 1, 6-dioxaspiro[4, 4]nonane and tetrahydrofuran alcohols, the relative yields being determined by the structure of the initial furan alcohol and the type of catalyst.
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For Part XXXII see [1].
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Ponomarev, A.A., Peshekhonova, A.D. Research on furan compounds. Chem Heterocycl Compd 3, 611–616 (1967). https://doi.org/10.1007/BF00468325
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DOI: https://doi.org/10.1007/BF00468325