Synthesis of a Key Intermediate of Novel Galbonolide Analogues via Efficient Construction of a Conjugated Diene System
スポンサーリンク
概要
- 論文の詳細を見る
The development of an efficient synthetic method enabled multi-gram synthesis of a key intermediate, which is useful for the modification at the C6-functional group of galbonolide analogues. The structure of a key intermediate including a conjugated diene was afforded by Horner-Emmons reaction, alkylation of Weinreb amide with alkyl lithium and a subsequent Wittig reaction.
- 公益社団法人日本薬学会の論文
- 2004-08-01
著者
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SATO Hiromi
Tohoku College of Pharmacy
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SAKOH Hiroki
Banyu Tsukuba Research Institute
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SAKURABA Shunji
Banyu Tsukuba Research Institute
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IMAMURA Hideaki
Banyu Tsukuba Research Institute
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SUGIMOTO Yuichi
Banyu Tsukuba Research Institute
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YAMADA Koji
Banyu Tsukuba Research Institute
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MORISHIMA Hajime
Banyu Tsukuba Research Institute
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Sato H
Banyu Tsukuba Research Institute Banyu Pharmaceutical Co. Ltd.
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JONA Hideki
Banyu Tsukuba Research Institute, Banyu Pharmaceutical Co., Ltd.
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Sugimoto Yoshikazu
Hanno Research Center Taiho Pharmaceutical Co. Ltd.
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Yamada K
Graduate School Of Pharmaceutical Sciences Kyushu University
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Jona H
Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo
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Jona H
Banyu Tsukuba Research Institute Banyu Pharmaceutical Co. Ltd.
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Jona Hideki
Banyu Tsukuba Research Institute
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Yamada Katsuya
Graduate School Of Pharmaceutical Sciences Nagoya City University
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Sakuraba S
Banyu Tsukuba Research Institute Banyu Pharmaceutical Co. Ltd.
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Sugimoto Yuichi
Banyu Tsukuba Research Institute Banyu Pharmaceutical Co. Ltd.
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Sakoh H
Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo
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Yamada Kenji
Tokyo University Of Pharmacy And Life Sciences School Of Pharmacy
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Morishima H
Banyu Tsukuba Research Institute Banyu Pharmaceutical Co. Ltd.
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Imamura H
Banyu Tsukuba Research Institute Banyu Pharmaceutical Co. Ltd.
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