Biochemical Preparation of Optically Active 4-Hydroxy-β-ionone and Its Transformation to (S)-6-Hydroxy-α-ionone(Organic Chemistry)
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概要
- 論文の詳細を見る
The preparation of 4-hydroxy-β-ionone of high enantiomeric excess was achieved via lipase-catalyzed transesterification of the corresponding racemate as the key-step. Starting from Its (R)-enantiomer, (S)-6-hydroxY-α-ionone, an important intermediate for synthetic abscisic acid analogs, was synthesized.
- 社団法人日本農芸化学会の論文
- 1991-07-23
著者
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Ohta Hiromichi
Department Of Chemistry Faculty Of Science And Technology Keio University
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SUGAI Takeshi
Department of Chemistry, Faculty of Science and Technology, Keio University
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Ohta Hiromichi
Department Of' Chemistry Keio University
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KAKEYA Hideaki
Department of Chemistry, Keio University
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Ohta H
Keio Univ. Yokohama Jpn
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Ohta Hiromichi
Department Of Applied Chemistry School Of Engineering Nagoya University
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Kakeya H
Antibiotics Laboratory Advanced Science Institute Riken
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Sugai T
Keio Univ. Yokohama Jpn
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Kakeya Hideaki
Department Of' Chemistry Keio University
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Kakeya H
Riken Saitama Jpn
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Kakeya Hideaki
Antibiotics Laboratory Advanced Science Institute Riken
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Sugai Takeshi
Department Of Agricultural Chemistry The University Of Tokyo
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