Yamauchi Satoshi | College Of Agriculture Ehime University

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概要

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著作論文

Improved Stereoselective Synthesis of Optically Active Methylene Lactone, Key Intermediate for the Synthesis of 1,2-Oxidized Furofuran Lignan, by Direct α-Methylenation to Butanolide
Stereoselective Synthesis of the Optically Active Samin Type of Lignan from L-Glutamic Acid
Stereoselective Synthesis of Optically Active Methylene Lactone, Key Intermediate for the Synthesis of 1,2-Oxidized Furofuran Lignan, from L-Glutamic Acid
Germination Inhibitor in Citrus unshu Fruit Peelings : ( + )-Abscisyl β-D-Glucopyranoside
Stereoselectivity in the Michael Addition Reaction of Dialkylcuprates to the 2-Cyclohexenones with C-4 Ester Substituents
Synthesis of (+)-(1S, 2S, 5R, 6S)-1-Hydroxysamin from L-(+)-Arabinose
Synthesis of 1,2-Oxygenated 6-arylfurofuran Lignan : Stereoselective Synthesis of (1S,2S,5R,6S)-1-hydroxysamin(Organic Chemistry)
Stereoselective Model Synthesis of the Optically Active Olivil Type of Lignan from D-Xylose
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

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