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- W2028587837 abstract "Optically active trans-tert-butyl-2-aminocyclopentylcarbamate (1) has potential utility as a scaffold for chiral ligands and as a modified backbone unit for peptide nucleic acids (PNAs). We have developed a short and practical synthesis of 1 via aziridine opening of tosyl-activated cyclopentene aziridine 2 and optical resolution of racemic 1 with 10-camphorsulfonic acid (CSA). The route provides ready access to multigram quantities of both enantiomers without the need for chromatography." @default.
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- W2028587837 date "2006-10-01" @default.
- W2028587837 modified "2023-09-26" @default.
- W2028587837 title "Practical Synthesis of <i>trans</i>-<i>tert</i>-Butyl-2-aminocyclopentylcarbamate and Resolution of Enantiomers" @default.
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- W2028587837 doi "https://doi.org/10.1021/jo061409v" @default.
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