189191-23-9Relevant articles and documents
Switchover of diastereofacial selectivity in the condensation reaction of optically active N-sulfinimine with ester enolate
Fujisawa, Tamotsu,Kooriyama, Yuuji,Shimizu, Makoto
, p. 3881 - 3884 (2007/10/03)
Both diastereomers of β-aminoester can be obtained diastereoselectively in the reaction of optically active N-sulfinimine possessing 2-methyl-1,3- dioxolanyl group with ester enolate simply by changing the enolate metal species, additives, and solvents. The β-aminoester can be converted into the corresponding 3-unsubstituted β-lactam.