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• W2089254240 abstract "Enantiomerically pure (l)-tryptophanol (5) was synthesized from 4(R)-iodomethyl-2-oxazolidinone (2) and indolylmagnesium bromide in three steps (52% overall yield). Using this procedure, we also prepared various tryptophanols with substituent(s) on the indole ring. Furthermore, optically active 4(R)-iodomethyl-2-oxazolidinone was readily prepared from an enantiomerically pure aziridine-2(S)-methanol in high yield. [reaction: see text]" @default.
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• W2089254240 date "2001-11-30" @default.
• W2089254240 modified "2023-10-16" @default.
• W2089254240 title "Synthesis of Substituted-(<i>l</i>)-Tryptophanols from an Enantiomerically Pure Aziridine-2-methanol" @default.
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• W2089254240 doi "https://doi.org/10.1021/ol016861+" @default.
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