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- W2152400843 abstract "This review mentions the total sytheses of the highly functionalized natural products, pederine, aplasmomycin, and virantmycin. The total synthesis of pederine was accomplished by employing the new method for stereocontrolled formation of N- (α-methoxyalkyl) amide. Based on the novel remote controlled asymmetric redutions of some chiral ketones, the formal total synthesis of aplasmomycin was achieved. The stereospecific total synthesis of virantmycin and its diastereomer were performed by using intramolecular addition reaction of nitrene to olefin, and relative stereochemistry of virantmycin was established unambiguouly." @default.
- W2152400843 created "2016-06-24" @default.
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- W2152400843 date "2010-08-19" @default.
- W2152400843 modified "2023-09-25" @default.
- W2152400843 title "ChemInform Abstract: Total Syntheses of Highly Functionalized Natural Products" @default.
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- W2152400843 doi "https://doi.org/10.1002/chin.199352328" @default.
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