Diastereoselective synthesis of bis(α-aminophosphonates) by lipase catalytic promiscuity
Author:
Affiliation:
1. Ecocompatible Asymmetric Catalysis Laboratory (LCAE)
2. Badji Mokhtar Annaba-University
3. 23000 Annaba
4. Algeria
5. Equipe de Catalyse Moléculaire
6. ICMMO
7. UMR CNRS
8. Bât 420
9. Université Paris-Sud
Abstract
New bis(α-aminophosphonates) were directly prepared with high diastereoselectivity by lipase catalytic promiscuity in the presence of immobilized Candida antarctica lipase.
Funder
Ministère de l'Enseignement Supérieur et de la Recherche Scientifique
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C8NJ06235H
Reference73 articles.
1. Stereodivergent Synthesis of Two Novel α-Aminophosphonic Acids Characterised by a cis-Fused Octahydroindole System
2. Renin inhibitors. Synthesis of transition-state analog inhibitors containing phosphorus acid derivatives at the scissile bond
3. Aminophosphonic Acids of Potential Medical Importance
4. Remarkable Potential of the α-Aminophosphonate/Phosphinate Structural Motif in Medicinal Chemistry
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