Highly Stereoselective Synthesis of (E)-Substituted Allylsilanes via the Still-Wittig Rearrangement
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概要
- 論文の詳細を見る
(E)-and(Z)-Vinylsilanes for the Still-Wittig rearrangement were easily prepared from propargyl alcohol 4. The Still-Wittig rearrangement of (Z)-vinylsilane 1d afforded (E)-allylsilane 3d stereoselectively. The stereoselectivity of (E)-vinylsilane, however, was unexpectedly low.
- 社団法人日本農芸化学会の論文
- 1997-08-23
著者
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Suzuki Yoshihiro
Graduate School Of Bioagricultural Sciences Nagoya University
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SAKAGAMI Youji
Department of Biological Sciences, Nagoya University
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Sakagami Y
Nagoya Univ. Nagoya Jpn
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Sakagami Youji
Department Of Agricultural Chemistry Nagoya University
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HARA Osamu
Department of Biology, Aichi University of Education
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FUJII Kazushige
Department of Applied Biological Sciences, Nagoya University
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Fujii K
Kinki Univ. Nara Jpn
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Hara Osamu
Department Of Applied Biological Sciences Nagoya University:(present Address)faculty Of Pharmaceutic
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Suzuki Yoshihiro
Graduate School of Bioagricultural Sciences, Nagoya University
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