107016-45-5

Upstream product

• 130849-20-6 (1-Amino-2-phenyl-ethyl)-methyl-phosphinic acid isopropyl ester 
• 108-88-3 toluene 
• 130849-12-6 Methyl-(2-phenyl-1-{[1-phenyl-meth-(E)-ylidene]-amino}-ethyl)-phosphinic acid isopropyl ester 
• 100-39-0 benzyl bromide 
• 126410-33-1 (1-Benzyloxycarbonylamino-2-phenyl-ethyl)-phosphinic acid methyl ester 
• 156336-14-0 methyl <1(R/S)-(N-CBZ-amino)-2-phenylethyl>methylphosphinate 
• 119012-13-4 <1(R/S)-(N-CBZ-amino)-2-phenylethyl>methylphosphinic acid 

Relevant academic research and scientific papers

Antibody-catalyzed hydrolysis of an unsubstituted amide

The generation of antibodies capable of catalyzing the unassisted hydrolysis of unactivated amides has been an enduring goal of research in the field. Antidialkylphosphinate 1 monoclonal antibodies were screened for their ability to catalyze the hydrolysi

ORGANIC PHOSPHORUS COMPOUNDS 91. SYNTHESIS AND PROPERTIES OF 1-AMINO-2-ARYLETHYLPHOSPHONIC AND -PHOSPHINIC ACIDS AS WELL AS -PHOSPHINE OXIDES

The preparation, physical and spectroscopic properties of 1-amino-2-arylethylphosphonic, and -phosphinic acids as well as -phosphine oxides, the phosphorus analogues of phenylalanine are described, and the reactions of 1-amino-2-(4-fluorophenyl)ethylphosphonates with acetals, isocyanides, esters, acid anhydrides, activated aromatic nitro- and halogen compounds, and with N-protected alanine are reported.It is shown that several of the 1-amino-2-arylethylphosphonic acids are strong inhibitors of PAL and anthocyanin synthesis and also are quite active botryticides.Among the active compounds were 1-amino-2-(4-fluorophenyl)ethylphosphonic acid, 3f, and the methyl-substituted compounds 3k, 3l, and 3m.The fluoroderivative 3f was also effective as a seed-dressing agent in barley showing a 100percent protection against the fungus Fusarium nivale at 600 ppm.