Asymmetric reduction with C1- and C2-symmetric NADH model compounds containing chiral 1,1'-binaphthyls.
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概要
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The present study deals with Mg-catalyzed asymmetric reduction of ethyl benzoylformate by the use of C<SUB>2</SUB>-symmetric NADH model compounds in which axial dissymmetry (chiral 1, 1′-binaphthyl derivatives) was introduced as a chiral source for the first time and the results were compared with those obtained by the corresponding C<SUB>1</SUB>-symmetric models bearing the same chiral center. Better e.e.'s of the reduction product were obtained by the use of NADH models having C<SUB>2</SUB>-symmetry than does the corresponding C<SUB>1</SUB> symmetric ones. Further, the kind of bonding as well as the distance between chiral binaphthyl and the reaction center affected the stereochemical course of hydrogen transfer.
- 公益社団法人 日本化学会の論文
著者
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Baba Naomichi
Institute For Chemical Research Kyoto University
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WATANABE Motoshi
Institute for Chemical Research, Kyoto University
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INOUYE Yuzo
Institute for Chemical Research, Kyoto University
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AMANO Masaki
Institute for Chemical Research, Kyoto University
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