H. Ambrosi, W. Duczek, M. Ramm
Oct 10, 1994
Citations
0
Influential Citations
5
Citations
Journal
Tetrahedron Letters
Abstract
Abstract Hydrogenation of 1-benzyl-aziridine-2-carboxylic acid ethyl ester 1 yielded the enantiomerically pure 1H-aziridine 2 or the β-amino acid ester 3 as main products depending on the reaction time. The Z-protected derivatives of 2 and 3 were transformed into the γ-lactones 4 and 5, respectively.