Agricultural and Biological Chemistry
Online ISSN : 1881-1280
Print ISSN : 0002-1369
ISSN-L : 0002-1369
Syntheses of Unsaturated Lactones
Part II. Flavorous Nature of Some 4- and 5-Substituted-5-Hydroxy-2-Enoic Acid Lactones
Akio NOBUHARA
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1969 年 33 巻 2 号 p. 225-229

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Homologous 4- and 5-substituted 5-hydroxy-2-enoic acid lactone were prepared, and the nature of their flavors as a butter cake flavor was investigated. Among those, unsaturated lactones having the best flavorous nature have the following structural properties. The length of a substituted residue at the γ-position of the lactone ring should be a short as possible. The lactones have a n-amyl residue at the δ-positio, and the total carbon number of a compound is ten. Namely, a compound is so better as to have a structure similar to that of 5-hydroxy-2-decenoic acid lactone.
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© Japan Society for Bioscience, Biotechnology, and Agrochemistry
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