Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Organic Chemistry Notes
Synthesis and Lateral Root-Inducing Activity of Novel N-Substituted-2-Piperidones with a 1,4-Benzodioxan Ring
Hidetaka TSUKADANaotaka YAMADAEiji TANIGUCHIEiichi KUWANO
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2000 年 64 巻 10 号 p. 2229-2231

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  Novel N-substituted-2-piperidones with a 1,4-benzodioxan ring were prepared and evaluated for their activity to induce lateral roots in lettuce seedlings. Compounds were obtained by aldol condensation of the lithium enolate of N-substituted-2-piperidones with 1,4-benzodioxan-6-carbaldehyde. Of the series compounds tested, N-cinnamyl-3-[1-(1,4-benzodioxan-6-yl)-1-hydroxymethyl]-2-piperidone (2e) had the highest activity. In seedlings treated with 10 ppm of 2e, all of the primary roots formed lateral roots. Only erythro-2e showed lateral root-inducing activity, while threo-2e was inactive.
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© 2000 by Japan Society for Bioscience, Biotechnology, and Agrochemistry
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