Facile entry to (-)-(R)- and (+)-(S)-mexiletine

35Citations
Citations of this article
11Readers
Mendeley users who have this article in their library.
Get full text

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free