Stereoselective Synthesis of (2S, 3S)-2-Benzy1-2-hydroxy-3-(3, 4-methylenedioxybenzyl)-γ-butyrolactone from L-(+)-Arabinose via a Carissanol-type of Lignan
スポンサーリンク
概要
- 論文の詳細を見る
As a model experiment for the synthesis of optically active α, β-dibenzyl-α-hydroxy-γ-butyrolactone (1), (2S, 3S)-2-benzyl-2-hydroxy-3-(3, 4-methylenedioxybenzyl)-γ-butyrolactone (3) was stereoselectively synthesized from L-(+)-arabinose via the carissanol-type of lignan, (2R/S, 3S, 4S)-3-benzyl-2, 3-dihydroxy-4-(3, 4-methylenedioxybenzyl)tetrahydrofuran (4).
- 社団法人日本農芸化学会の論文
- 1998-03-23
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
関連論文
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- Stereoselective Synthesis of Optically Active Methylene Lactone, Key Intermediate for the Synthesis of 1,2-Oxidized Furofuran Lignan, from L-Glutamic Acid
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- Stereoselective Syntheses of (-)-Podorhizol Lignan and its Derivatives : erythro and threo Preferential Aldol Condensation of Potassium Enolate from γ-Butyrolactone with Alkoxybenzaldehyde
- First Stereoselective Synthesis of (+)-Magnostellin C, a Tetrahydrofuran Type of Lignan Bearing a Chiral Secondary Benzyl Alcohol(Organic Chemistry)
- Stereoselective Synthesis of (2S, 3S)-2-Benzy1-2-hydroxy-3-(3, 4-methylenedioxybenzyl)-γ-butyrolactone from L-(+)-Arabinose via a Carissanol-type of Lignan
- 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