Biomimetic Syntheses of Isodityrosine Natural Products, and an Approach to Chemistry and Molecular Recognition of Secoaglucovancomycin and Related Oligopeptides
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概要
- 論文の詳細を見る
The biomimetic oxidation of dihalogenated phenols employing TTN or electrolysis, effected the construction of a diaryl ether linkage, leading to the syntheses of isodityrosine natural products. In particular, the halogen substituents were found to control the oxidation-direction. The vancomycin derivatives were also synthesized, and their interaction to models of bacterial cell wall precursors were observed by NMR techniques, coupled with the theoretical calculations.
- 社団法人 有機合成化学協会の論文
- 1997-11-01
著者
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Yamamura Shosuke
Department Of Chemistry Faculty Of Science And Technology Keio University
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Nishiyama Shigeru
Department Of Chemistry Faculty Of Science And Technology Keio University
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Nishiyama Shigeru
Department Of Chemistry Faculty Of Science And Technology Keio Univerisity
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