Abstract
The resolution of 1-cyclohexylethylamine 1 with enantiopure 2-phenylacetic acids via diastereomeric salt formation was investigated. ( R)-2-Methoxy-2-phenylacetic acid 3 and the ( S)-2-phenylpropionic acid 5 were found to be efficient resolving agents for obtaining the single enantiomer ( S)- 1 as the correspondingly less-soluble diastereomeric salt (resolution efficiency = 48% and 52%, respectively).
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
