10 サフラマイシン系抗生物質の合成研究 : 光学活性サフラマイシンMx2の全合成(口頭発表の部)
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概要
- 論文の詳細を見る
Saframycin Mx 2 4b was discovered in the culture broth of the myxobacterium, Myxococcus xanthus in 1988. It is interesting that this compound has a quinone moiety on the E-ring and a hydroquinone, because the only successful total synthesis within the saframycin family has been of the bisquinone series. We describe first the transformation of (-)-saframycin A 1a to the saframycin Mx type compound (-)-15 and the synthesis of saframycin E 1e, whose structure has not yet been established because of its instability, from saframycin B 1b. Next, we described the first total synthesis of (-)-N-acetylsaframycin Mx 2 25a from (±)-pentacyclic amine 17, which was a key intermediate of our (±)-saframycin synthesis. The reaction of 17 with Cbz-L-alanine gave a mixture of amides (-)-18a and (-)-18b. Deprotection and acetylation of (-)-18a and (-)-18b produced amides (-)-20a and (-)-20b, respectively. The structure of (-)-20b was determined by X-ray crystallography. The conversion of (-)-20a to the bisquinone (-)-21a and subsequent stereoselective and regioselective introduction of the methoxyl group at position 5 provided (-)-22a. Finally, (-)-22a was subjected to catalytic reduction and regioselective oxidation to give (-)-25a in modest yield. The epi-enantiomer (-)-18b was transformed to (+)-25b in a same four-step sequence. The specific optical rotation and the CD spectra of (-)-25a and (+)-25b were of opposite signs.
- 天然有機化合物討論会の論文
- 1995-09-01
著者
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山口 健太郎
千葉大学分析センター
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齋藤 直樹
Meiji Pharmaceutical University
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齋藤 直樹
明治薬科大学
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原田 俊司
明治薬科大学
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西田 昌代
明治薬科大学
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井上 泉
明治薬科大学
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久保 陽徳
明治薬科大学
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原田 俊司
Meiji College of Pharmacy
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西田 昌代
Meiji College of Pharmacy
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井上 泉
Meiji College of Pharmacy
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Nishida Makiko
崇城大学 薬学部薬学科
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Nishida Makiko
Faculty Of Engineering Kyushu Kyoritsu University
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Nishida M
Department Of Clinical Pharmacy Faculty Of Pharmacy Meijo University
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Kubo Akinori
Graduate School Of Pharmaceutical Sciences Meiji Pharmaceutical University
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NISHIDA Miharu
Department of Analytical Chemistry of Medicines, Showa Pharmaceutical University
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