942631-71-2

Upstream product

• 884489-24-1 diethyl [1-(3,4-dichlorophenyl)-2-formylethyl]phosphonate 
• 622-33-3 N-benzyloxyamine 
• 62374-02-1 (E)-3,4-dichlorocinnamaldehyde 
• 884489-20-7 diethyl [1-(3,4-dichlorophenyl)-3,3-diphenoxypropyl]phosphonate 

Downstream Products

• 884489-38-7 diethyl 3-(N-(benzyloxy)acetamido)-1-(3,4-dichlorophenyl)propylphosphonate 
• 884489-34-3 diethyl 3-(N-(benzyloxy)formamido)-1-(3,4-dichlorophenyl)propylphosphonate 
• 884489-43-4 diethyl [3-(N-hydroxyacetamido)-1-(3,4-dichlorophenyl)propyl]phosphonate 
• 884489-39-8 diethyl [1-(3,4-dichlorophenyl)-3-(N-hydroxyformamido)propyl]phosphonate 
• 884489-32-1 [3-benzyloxyamino-1-(3,4-dichlorophenyl)-propyl]-phosphonic acid diethyl ester 

Relevant academic research and scientific papers

ORGANOPHOSPHORIC DERIVATIVES USEFUL AS ANTI-PARASITIC AGENTS

The present invention relates to novel phosphonic acid compounds having the structural formula (I): wherein: (a) R is a group of 1 to 5 substituents independently selected from the group consisting of fluoro, chloro, bromo, C1-4 alkoxy, C1

Synthesis of α-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors

In view of the promising antimalarial activity of fosmidomycin or its N-acetyl homologue FR900098, the objective of this work was to investigate the influence of aromatic substituents in the α-position of the phosphonate moiety. The envisaged analogues we