Synthesis of Optically Active Olivil Type of Lignan from L-Arabinose Using threo-Selective Aldol Condensation as a Key Reaction
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概要
- 論文の詳細を見る
The threo-selective aldol condensation of (3R, 4S) -3-hydroxy-5-trityloxy-4-pentanolide, which was prepared from L-arabinose, with piperonal was applied to the stereoselective synthesis of the olivil type of lignan, (2R, 3R, 4R) -4-benzyl-4-hydroxy-3-hydroxymethyl-2-(3,4-methylenedioxyphenyl) tetrahydrofuran.
- 社団法人日本農芸化学会の論文
- 2000-11-23
著者
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YAMAUCHI Satoshi
College of Agriculture, Ehime University
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Kinoshita Yoshiro
College Of Agriculture Ehime University
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Yamauchi Satoshi
College Of Agriculture Ehime University
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Kinoshita Yoshiro
College Of Agricullture Ehime University
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Yamauchi Satoshi
College Of Agricullture Ehime University
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- Synthesis of cis-Lactone Lignan, cis-(2S, 3R)-Parabenzlactone, from L-Arabinose(Organic Chemistry)
- Synthesis of Optically Active Olivil Type of Lignan from L-Arabinose Using threo-Selective Aldol Condensation as a Key Reaction
- Stereoselective Synthesis of (2R, 3S)-2-Benzyl-2-hydroxy-3-(3,4-methylenedioxybenzyl)-γ-butyrolactone from L-(+)-Arabinose