Total synthesis of pacidamycin D by Cu(I)-catalyzed oxy enamide formation |
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Authors: | Okamoto Kazuya Sakagami Masahiro Feng Fei Togame Hiroko Takemoto Hiroshi Ichikawa Satoshi Matsuda Akira |
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Affiliation: | Shionogi Innovation Center for Drug Discovery, Shionogi & Co., Ltd., Kita-21 Nishi-11, Sapporo 001-0021, Japan. |
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Abstract: | The first total synthesis of pacidamycin D, which is expected to be a good candidate as an antibacterial agent against P. aeruginosa, is described. The key elements of our approach feature an efficient and stereocontrolled construction of the Z-oxyvinyl iodide and copper-catalyzed cross-coupling with the tetrapeptide carboxamide. |
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