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- W2017384401 abstract "Abstract A new synthesis of stereochemically pure (L)-4-fluorotryptophan [i.e., (2S)-4-fluorotryptophan] in seven steps from 4-fluoroindole is described. A key reaction in the synthetic strategy is a diastereoselective alkylation of the Schollkopf chiral auxiliary with a fluorinated electrophile. All reaction steps are efficient and proceed in at least 80% yield. Keywords: Asymmetric synthesisfluoroamino acids4-fluorotryptophanorganofluorine chemistry" @default.
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- W2017384401 date "2011-09-14" @default.
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- W2017384401 title "Synthesis of (L)-4-Fluorotryptophan" @default.
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- W2017384401 doi "https://doi.org/10.1080/00397911.2010.523154" @default.
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