Abstract
AbstractStereoselectivity in the mutual kinetic resolution (KR) of racemic 3,4‐dihydro‐3‐methyl‐2H‐[1,4]benzoxazines and racemic 2‐aryloxy propionyl chlorides was studied. Based on the results obtained, preparative methods for single enantiomers of a series of 2‐aryloxy propionic acids via acylative KR of their racemates with enantiopure (S)‐3,4‐dihydro‐3‐methyl‐2H‐[1,4]benzoxazines have been proposed.
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