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- W1988550292 abstract "Asymmetric first total synthesis of eudistomidins G, H, and I, tetrahydro-β-carboline alkaloids from the Okinawan marine tunicate Eudistoma glaucus, has been accomplished with the Bischler–Napieralski reaction and the Noyori catalytic asymmetric hydrogen-transfer reaction. The absolute configurations of eudistomidins G, H, and I were confirmed from comparison of the 1H and 13C NMR, and CD spectral data of synthetic and natural eudistomidins G, H, and I, respectively." @default.
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- W1988550292 date "2012-08-01" @default.
- W1988550292 modified "2023-10-14" @default.
- W1988550292 title "Enantioselective total synthesis of eudistomidins G, H, and I" @default.
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- W1988550292 doi "https://doi.org/10.1016/j.tet.2012.05.071" @default.
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