The Journal of Antibiotics
Online ISSN : 1881-1469
Print ISSN : 0021-8820
ISSN-L : 0021-8820
Synthesis of Milbemycins α9, α10, α11, α12, α14, α15, α20, α21, α22, α23, α26, α27, Δ2, 3, Δ4, 26-Milbemycins A3, A4 from Milbemycins
TAKAHIRO TSUKIYAMAHISAKI KAJINOFUMIE KAJINOSATORU FURUTAYOSHIHISA TSUKAMOTOKAZUO SATOAYAKO KINOSHITAREIJI ICHINOSEKEIJI TANAKA
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2002 Volume 55 Issue 11 Pages 993-1003

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Abstract

Chemical derivation methods to prepare 26-acyloxy and 26-hydroxymilbemycins, which had been reported as natural products, milbemycins α9, α10, α11, α12, α14, α15, α20, α21, α22, α23, α26, α27 from milbemycins A3, A4 were reported. Δ2, 3, Δ4, 26-Milbemycins A3, A4, which had also been reported as natural products, were further prepared from milbemycins A3, A4. Their acaricidal activities were also assessed against the organophosphorus-sensitive two-spotted spider mite (Tetranychus urticae) on primary leaves of cowpea plants (Vigna sinesis Savi species) by spraying.

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