Literature DB >> 31729883

Enantioselective Aza-Reformatsky Reaction with Ketimines.

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


  2 in total

Review 1.  Hydroxy- and Amino-Phosphonates and -Bisphosphonates: Synthetic Methods and Their Biological Applications.

Authors:  Babak Kaboudin; Payam Daliri; Samaneh Faghih; Hesam Esfandiari
Journal:  Front Chem       Date:  2022-06-01       Impact factor: 5.545

Review 2.  Asymmetric Synthesis of Tetrasubstituted α-Aminophosphonic Acid Derivatives.

Authors:  Aitor Maestro; Xabier Del Corte; Adrián López-Francés; Edorta Martínez de Marigorta; Francisco Palacios; Javier Vicario
Journal:  Molecules       Date:  2021-05-27       Impact factor: 4.411

  2 in total

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