Enantioselective Synthesis of the (1S,5R)-Enantiomer of Litseaverticillols A and B
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概要
- 論文の詳細を見る
An enantioselective synthesis of the (1S,5R)-enantiomer of litseaverticillols A and B was accomplished in line with our previously reported synthetic pathway for their (1R,5S)-enantiomer. The use of “EtSCeCl2” prepared from EtSLi and CeCl3, instead of previously employed EtSLi itself, for the formation of thiol ester intermediates prevented any undesirable epimerization occurring in the process.
- 社団法人 日本農芸化学会の論文
- 2006-10-23
著者
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Kuwahara Shigefumi
Laboratory Of Agricultural Chemicals Faculty Of Agriculture Ibaraki University
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Kiyota Hiromasa
Laboratory Of Applied Bioorganic Chemistry Division Of Bioscience & Biotechnology For Future Bio
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Kiyota Hiromasa
Laboratory Of Applied Bioorganic Chemistry Graduate School Of Agricultural Science Tohoku University
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MORITA Akira
Laboratory of Applied Bioorganic Chemistry, Graduate School of Agricultural Science, Tohoku Universi
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Kuwahara Shigefumi
Laboratory Of Applied Bioorganic Chemistry Graduate School Of Agricultural Science Tohoku University
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Morita Akira
Laboratory Of Applied Bioorganic Chemistry Graduate School Of Agricultural Science Tohoku University
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