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• W2020050920 abstract "A stereospecific synthesis of both enantiomers of the marine alkaloid eudistomin X using the amino acid chiral pool is achieved. Comparison of 1H and 13C NMR chemical shifts of the synthetic product as either the free base, mono-salt or disalt with those reported for the natural product established that the ascidian metabolite was originally characterised as a mono-salt and that the absolute configuration was (10R)." @default.
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• W2020050920 date "2011-02-01" @default.
• W2020050920 modified "2023-09-27" @default.
• W2020050920 title "Establishment of the absolute configuration of the bioactive marine alkaloid eudistomin X by stereospecific synthesis" @default.
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• W2020050920 doi "https://doi.org/10.1016/j.tetlet.2010.12.052" @default.
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