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https://doi.org/10.1016/s0040-4039(00)92366-9
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Cite Journal: Tetrahedron Letters |  Publication Date: Sep 1, 1991 |
 Citations: 103 |
Affiliation: Harvard University
The reaction of S-tert-butyl thiopropionate with a number of N-benzyl or N-allyl aldimines ( 4) as promoted by the chiral diazaborolidine 1 and triethylamine afforded the β-amino acid esters 5 with high diastereoselectivity and enantioselectivity, providing a simple route to chiral β-lactams 6.
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