Optically active α-aminoalkylphosphonic acids 1 are structural analogues of α-amino acids
2, obtained by isosteric substitution of the planar and less bulky carboxylic acid (CO 2 H) by …

A wide range of methods for the enantioselective synthesis of α‐aminophosphonic acid
derivatives have been developed over the years. Although the most used methodology is …

A series of 20 novel α‐aminophosphonate derivatives bearing quinoline or quinolone
moiety was designed and synthesized via Kabachnik‐Fields reaction in the presence of …

A highly efficient one-pot multi-component reaction (MCR) protocol over DTP/SiO2 has been
developed for the synthesis of α-aminophosphonate derivatives (4a–x) in excellent yields …

An efficient and simple approach has been developed for the synthesis of eight dialkyl/aryl
[(5-phenyl-1, 3, 4-oxadiazol-2-ylamino)(aryl) methyl] phosphonates through the Pudovik …

Two silver (I) complexes, bis {diethyl [(5-phenyl-1, 3, 4-oxadiazol-2-yl-κ N 3: κ N 4-amino)(4-
trifluoromethylphenyl) methyl] phosphonate-(tetrafluoroborato-κ F)}-di-silver (I) and tetrakis …

The design and application of environmental-friendly catalysts to reduce the toxic wastes are
critical for improving the chemical synthesis. Therefore, copper (II)-β-cyclodextrin catalyst …

The naturally viable α-amino acid surrogates have been synthesised via Kabachnik–Fields
reaction by the condensation of 2-aminothiazole with various aldehydes and dialkyl …

A series of new α‐sulfamidophosphonate/sulfonamidophosphonate (4a–n) and
cyclosulfamidophosphonate (5a–d) derivatives containing the quinoline or quinolone moiety …

The review discusses recent achievements in the development of more ecofriendly and
economically viable processes for the synthesis of biologically potent α-aminophosphonates …