One-Pot Synthesis and Antimicrobial Activity of Novel α-Aminophosphonates Using TMG [PDF]
α-Aminophosphonates (4a-j) were synthesized in one-pot simultaneous reaction of 4-bromo-3-methyl benzenamine (1), dimethylphosphite (3) and different aromatic aldehydes (2a-j) by Kabachnik-Fields reaction in the presence of tetramethylguanidine (TMG) (10
B. Siva Kumar +3 more
doaj +3 more sources
Efficient synthesis of α-aminophosphonates using magnetically retrievable ionic nanocatalysts under ultrasound acceleration [PDF]
Magnetic supported ionic liquids are a unique subclass of ionic liquids that possess the ability to respond to external magnetic fields, combining the advantageous properties of traditional ILs with this magnetic responsiveness.
Farzaneh Saboury +3 more
doaj +2 more sources
Ru-Catalyzed Asymmetric Transfer Hydrogenation of α-iminophosphonates: A Novel Synthetic Approach for Valuable Chiral α-Aminophosphonates. [PDF]
This study reports the first Ru‐catalyzed ATH of α‐iminophosphonates, enabling the efficient synthesis of chiral α‐aminophosphonates. Both acyclic and cyclic substrates are converted in high yields (up to 97%) with excellent enantioselectivities (up to >99:1), offering a practical alternative to conventional AH for accessing phosphorus‐containing ...
Plouard P +8 more
europepmc +2 more sources
Catalyst-Free Cross-Dehydrogenative Coupling Strategy Using Air as an Oxidant: Synthesis of α‑Aminophosphonates [PDF]
Jayaraman Dhineshkumar +2 more
doaj +2 more sources
Asymmetric Transfer Hydrogenation as a Key Step in the Synthesis of the Phosphonic Acid Analogs of Aminocarboxylic Acids. [PDF]
The asymmetric transfer hydrogenation (ATH) of 17 diisopropyl α‐oxophosphonates was accomplished by using a commercially available Noyori‐type catalyst. The highly enantioenriched products (ee >98 % in all cases but one) were further converted to the phosphonic acid analogs of 15 aminocarboxylic acids.
Dinhof T +9 more
europepmc +2 more sources
Encouraged by the significant cytotoxic activity of simple α-aminophosphonates, a molecular library comprising phosphonoylmethyl- and phosphinoylmethyl-α-aminophosphonates, a tris derivative, and N-acylated species was established.
Petra R. Varga +4 more
doaj +1 more source
New Cytotoxic Derivatives by the Phosphorylation and Phosphinoylation of Diethyl α-Amino-α-Aryl-Methylphosphonates. [PDF]
In order to make available potentionally bioactive new α‐aminophosphonic derivatives, diethyl α‐amino‐α‐aryl‐methylphosphonates were phosphorylated, phosphinoylated and thiophosphinoylated with the corresponding P‐chloride. The effect of a P=O to P=S modification was evaluated by single crystal X‐ray cristallography.
Bircher M +6 more
europepmc +2 more sources
β-Hydrazonophosphine oxides are precursors of useful organophosphorus compounds, including phosphorylated N-heterocycles, α-aminophosphonates, and vinylphosphonates.
Alexandr O. Kokuev +1 more
doaj +1 more source
Microwave-assisted synthesis of α-aminophosphonates with sterically demanding α-aryl substituents [PDF]
A series of N-benzhydryl protected α-aminophosphonates with α-phenyl, α-(1-naphtyl), α-(9-anthryl) or α-(1-pyrenyl) substituents was synthesized by the Kabachnik–Fields condensation of diphenylmethylamine (benzhydrylamine), the corresponding aryl ...
Bálint, Erika +5 more
core +1 more source
A novel nanocomposite (N–TiO2-α-Am.Ph) was designed by surface functionalization of nano titanium oxide (N–TiO2) with α-aminophosphonates (α-Am.Ph). A study was aimed to explore and investigate the uptake properties of (N–TiO2-α-Am.Ph) for divalent Pb/Cu
Mohamed E. Mahmoud +2 more
doaj +1 more source

