Agricultural and Biological Chemistry
Online ISSN : 1881-1280
Print ISSN : 0002-1369
ISSN-L : 0002-1369
Chemical Studies on Ambergris
Part III. Synthesis of α-Ambrein-tetrahydropyranylether
Takayuki ORITANIMasanao MATSUI
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1966 年 30 巻 8 号 p. 759-763

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Dihydro-α-ionol (II) was converted to dihydro-α-ionyl bromide (III) and dihydro-α-ionyl tosylate (V), which afforded their Wittig reagents (IV), (VI) on heating with tri-phenylphosphine. The Wittig reaction of ambreinolal-tetrahydropyranylether (VII) with the above Wittig reagents (IV) or (VI) gave a-ambrein-tetrahydropyranylether (VIII).
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© Japan Society for Bioscience, Biotechnology, and Agrochemistry
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