Practical Synthesis of a Key Intermediate for Lactacystin from (R)-4-Hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl Acetate
スポンサーリンク
概要
- 論文の詳細を見る
A practical synthesis of a key intermediate for the proteasome inhibitor lactacystin from (R)-4-hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate was established. (R)-4-Hydroxymethyl-2-phenyl-4,5-dihydrooxazol-4-ylmethyl acetate is a useful chiral building block for the synthesis of biologically active compounds containing α-substituted α-amino acid moieties.
- 公益社団法人日本薬学会の論文
- 2008-05-01
著者
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Miyaoka Hiroaki
School Of Pharmacy Tokyo University Of Pharmacy And Life Sciences
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Miyaoka Hiroaki
School Of Pharmacy Tokyo University Of Pharmacy And Life Science
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MITOME Hidemichi
School of Pharmacy, Tokyo University of Pharmacy and Life Science
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MITOME Hidemichi
Faculty of Pharmaceutical Sciences, Matsuyama University
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KAWASHIMA Etsuko
School of Pharmacy, Tokyo University of Pharmacy and Life Sciences
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YAMANISHI Makoto
School of Pharmacy, Tokyo University of Pharmacy and Life Sciences
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HOSHINO Ayako
School of Pharmacy, Tokyo University of Pharmacy and Life Sciences
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Mitome Hidemichi
Faculty Of Pharmaceutical Sciences Matsuyama University
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Mitome Hidemichi
School Of Pharmacy Tokyo University Of Pharmacy And Life Science
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Hoshino Ayako
School Of Pharmacy Tokyo University Of Pharmacy And Life Sciences
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Yamanishi Makoto
School Of Pharmacy Tokyo University Of Pharmacy And Life Sciences
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Kawashima Etsuko
School Of Pharmacy Tokyo University Of Pharmacy And Life Sciences
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