143381-57-1Relevant articles and documents
Highly Stereodivergent Approach to Both Enantiomers of 4-Substituted β-Lactams via Diastereofacially Controlled Addition of Enolates of t-Butyl Acetate to a Chiral Imine
Shimizu, Makoto,Ukaji, Yutaka,Tanizaki, Junko,Fujisawa, Tamotsu
, p. 1349 - 1352 (2007/10/02)
Addition of lithium or triisopropoxytitanium enolate derived from t-butyl acetate to a chiral imine possessing dioxolane ring as a chiral auxiliary gave (3S)-β-amino ester exclusively, whereas chlorozinc enolate underwent re-facial attack to give (3R)-iso