@article{oai:kutarr.kochi-tech.ac.jp:00000195,
 author = {Hashimoto, Yukihiko and Ogasawara, Tsuneo and Hayashi, Minoru and Saigo, Kazuhiko},
 issue = {3},
 journal = {Heterocycles},
 month = {Jun},
 note = {Chiral imines, derived from (1S,2R)-2-methoxy-1,2-diphenylethyl-amine and aromatic aldehydes, reacted with ester enolates prepared from ketene silyl acetals and methyllithium to give β-lactams in good yields with high diastereoselectivity. This method provides a useful and simple route for the construction of optically active β-lactam skeletons.},
 pages = {1001--1004},
 title = {STEREOSELECTIVE SYNTHESIS OF OPTICALLY ACTIVE β-LACTAMS BY THE REACTION OF CHIRAL IMINES DERIVED FROM ERYTHRO-2-AMINO-1,2-DIPHENYLETHANOL WITH ESTER ENOLATES},
 volume = {52},
 year = {1905}
}