Studies on the Synthesis of Myriaporones : Stereoselective Synthesis of the C5-C13 Fragment Starting from D-Glucose via Regioselective Reductive Opening of Methoxybenzylidene Acetal
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概要
- 論文の詳細を見る
A stereoselective synthesis is described of the C5-C13 fragment (4) of myriaporone 4 (1) starting from D-glucose by a coupling of the C5-C9 aldehyde (5), prepared using a regioselective reductive ring-opening of methoxy-benzylidene acetal, with the C10-C13 iodoolefin (6).
- 公益社団法人日本薬学会の論文
- 2000-11-01
著者
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Zheng Bao-zhong
Department Of Chemistry Okayama University Of Science
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Yonemitsu Osamu
Departmen Of Chemistry Okayama University Of Science
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YAMAUCHI Megumi
Department of Chemistry, Okayama University of Science
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DEI Hiroo
Department of Chemistry, Okayama University of Science
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Dei Hiroo
Department Of Chemistry Okayama University Of Science
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Yamauchi Megumi
Department Of Chemistry Okayama University Of Science
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