Synthesis of Aminomethylene-gem-bisphosphonates Containing an Aziridine Motif: Studies of the Reaction Scope and Insight into the Mechanism
Author:
Affiliation:
1. Team Nucleosides & Phosphorylated Effectors, Institute for Biomolecules Max Mousseron (IBMM), UMR 5247 CNRS, ENSCM, Univ. Montpellier, Campus Triolet, cc1705, Place Eugène Bataillon, 34095 Montpellier, France
Funder
Centre National de la Recherche Scientifique
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c02434
Reference61 articles.
1. Nucleophilic ring opening reactions of aziridines
2. Synthesis of Functionalized Novel α ‐Amino‐ β ‐alkoxyphosphonates through Regioselective Ring Opening of Aziridine‐2‐phosphonates
3. Reaction of 2H-Azirine Phosphine Oxide and -Phosphonates with Nucleophiles. Stereoselective Synthesis of Functionalized Aziridines and α- and β-Aminophosphorus Derivatives
4. Synthetic Methods for Azaheterocyclic Phosphonates and Their Biological Activity
5. A Convenient Synthesis of Dialkyl [[2-(Bromomethyl)aziridin-1-yl]methyl]phosphonates, New Heterocyclic β-Azaphosphonates
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