| Literature DB >> 31729883 |
Aitor Maestro1, Edorta Martinez de Marigorta1, Francisco Palacios1, Javier Vicario1.
Abstract
Here, an enantioselective aza-Reformatsky reaction using acyclic ketimine substrates is presented. Using α-phosphorated ketimines as electrophilic substrates and a simple BINOL-derived ligand, phosphorated analogues of aspartic acid holding chiral tetrasubstituted carbons are efficiently obtained with excellent enantioselectivity through an asymmetric organocatalytic Reformatsky-type reaction. The phosphorated analogues of aspartic acid have been used for the synthesis of phosphorus-containing enantiopure tetrasubstituted β-lactams.Entities:
Year: 2019 PMID: 31729883 DOI: 10.1021/acs.orglett.9b03669
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005