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Total synthesis of xiamenmycin C and all of its stereoisomers: stereochemical revision

机译:厦门霉素C及其所有立体异构体的全合成:立体化学修订

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摘要

Xiamenmycin C, a potent anti-fibrotic natural product, and all of its stereoisomers have been synthesized and their structures were fully characterized. Based on this study, the originally proposed structure of xiamenmycin C has been accordingly revised to be 2R,3S.
机译:厦门霉素C是一种有效的抗纤维化天然产物,其所有立体异构体均已合成,并已对其结构进行了充分表征。在此基础上,厦门霉素C最初提出的结构已相应地修改为2R,3S。

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