Issue 0, 1967

Natural acetylenes. Part XXVI. Transformations of phenyl-polyacetylenes in the tubers of Dahlia hybrids

Abstract

The hydrocarbon trans-Ph·[C[triple bond, length half m-dash]C]2·CH[double bond, length half m-dash]CHMe (tritium-labelled in the benzene ring) was inserted into the tuberous roots of two Dahlia hybrids and found to be converted into the ω-alcohol trans-Ph·[C[triple bond, length half m-dash]C]2·CH[double bond, length half m-dash]CH·CH2·OH, the threo-diol Ph·[C[triple bond, length half m-dash]C]2·CH(OH)·CHMe·OH, and the threo-triol Ph·[C[triple bond, length half m-dash]C]2·CH(OH)·CH(OH)·CH2·OH, but not into the hydrocarbon Ph·[C[triple bond, length half m-dash]C]3·Me. The diol and triol had not previously been recognised as natural products.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 1038-1041

Natural acetylenes. Part XXVI. Transformations of phenyl-polyacetylenes in the tubers of Dahlia hybrids

E. R. H. Jones, S. Safe and V. Thaller, J. Chem. Soc. C, 1967, 1038 DOI: 10.1039/J39670001038

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