139255-87-1Relevant academic research and scientific papers
High diastereofacial selectivity in the 1,3-dipolar cycloaddition of chiral azomethine ylides
Deprez,Royer,Husson
, p. 1189 - 1192 (1991)
Excellent diastereofacial and endo/exo stereoselectivities have been obtained in cycloaddition of the chiral azomethine ylide generated from 4-phenyloxazolidine acetic acid (-)-8-phenylmenthyl ester 1e.
