2016
DOI: 10.1016/j.jfluchem.2016.03.014
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Synthesis of polyfluoroalkylated α-Aminophosphonic/thiophosphonic acids derivatives

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Cited by 7 publications
(3 citation statements)
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“…The 2-chloroethylureidophosphonate (AE)-20 was achieved with a 70% yield via nucleophilic addition of diethylamino(phenyl)methylphosphonate hydrochloride (AE)-19 with 2-chloroethyl isocyanate in basic conditions at 0 °C. 21 It was then treated with sodium nitrite (3 equiv.) using formic acid at low 0 °C in DCM for 2 hours.…”
Section: Chemistrymentioning
confidence: 99%
“…The 2-chloroethylureidophosphonate (AE)-20 was achieved with a 70% yield via nucleophilic addition of diethylamino(phenyl)methylphosphonate hydrochloride (AE)-19 with 2-chloroethyl isocyanate in basic conditions at 0 °C. 21 It was then treated with sodium nitrite (3 equiv.) using formic acid at low 0 °C in DCM for 2 hours.…”
Section: Chemistrymentioning
confidence: 99%
“…N-Sulfonyl and N-carboxylic imine derivatives were also applied as starting materials in the Pudovik reaction to prepare the corresponding α-aminophosphonates [134][135][136][137].…”
Section: Pudovik Reactions Of α-Aliphatic Iminesmentioning
confidence: 99%
“…Besides the diverse biological activities like enzyme inhibitors, antibiotics, or anticancer agents, substituted a-aminophosphonate derivatives have stimulated great interest as antiviral and antifungal agents and they have been extensively used as insecticides and herbicides. [19][20][21][22][23] Therefore, considering the biological values and possibilities in the chemical modication of a-amino-phosphonates, the growing concern and the development of new organophosphorus compounds are still of great interest. [24][25][26][27][28][29][30] Plant growth testgermination, growth inhibition, dry and fresh matter…”
Section: Ecotoxicological Activitymentioning
confidence: 99%