Abstract
The title compounds, 1a and 1b, have been synthesized in a three-step sequence starting from (-)-(S) and (+)-(R)-propylene oxide, respectively, in acceptable overall yields. The enantiomeric excess values for 1a and 1b were 96% and 93% respectively, as assessed by HPLC analysis on a chiral stationary phase of the corresponding N-acetyl derivatives. The synthetic route herein presented may represent a facile entry to highly enriched mexiletine enantiomers, alternative to those previously reported in the literature. (C) 2000 Wiley-Liss, Inc.
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Carocci, A., Franchini, C., Lentini, G., Loiodice, F., & Tortorella, V. (2000). Facile entry to (-)-(R)- and (+)-(S)-mexiletine. Chirality, 12(3), 103–106. https://doi.org/10.1002/(SICI)1520-636X(2000)12:3<103::AID-CHIR1>3.0.CO;2-X
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