Asymmetric Reduction of Aromatic Ketones with Chirally Modified Reagents Prepared from Sodium Borohydride and Optically Active Acids in the Presence of l, 2: 5, 6-Di-O-isopropylidene-α-D-glucofuranose
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概要
- 論文の詳細を見る
Asymmetric reduction of aromatic ketones using chirally modified reagents prepared from sodium borohydride and optically active acids in the presence or absence of 1, 2: 5, 6-di-O-isopropylidene-α-D-glucofuranose produced the corresponding optically active alcohols with optical yields of 447 %. The reagent prepared from sodium borohydride and 1 equivalent of l-malic acid in the presence of 2 equivalents of 1, 2: 5, 6-di-O-isopropylidene-α-D-glucofuranose gave the highest yields.
- 社団法人 日本農芸化学会の論文
著者
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Hirao Akira
Department Of Polymer Chemistry Tokyo Institute Of Technology
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Hirao A
Tokyo Inst. Technol. Tokyo Jpn
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Yamazaki Noboru
Department of Internal Medicine III
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NAKAHAMA Seiichi
Department of Polymer Chemistry, Tokyo Institute of Technology
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Hirao Akira
Department Of Agronomy Faculty Of Agriculture Tottori University
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MOCHIZUKI Hidenori
Department of Polymer Science, Tokyo Institute of Technology
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ZOOROB Hanafi
Department of Polymer Science, Tokyo Institute of Technology
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IGARASHI Ichiro
Department of Polymer Science, Tokyo Institute of Technology
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ITSUNO Shinichi
Department of Polymer Science, Tokyo Institute of Technology
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OHWA Masaki
Department of Polymer Science, Tokyo Institute of Technology
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Nakahama Seiichi
Department Of Organic And Polymeric Materials Graduate School Of Science And Engineering Tokyo Insti
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Yamazaki Noboru
Department Of Biomaterials And Devices Kanagawa Dental College
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ITSUNO Shinichi
Department of Environmental and Life Sciences, Toyohashi University of Technology
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