119552-92-0

Upstream product

• 63694-18-8 (+/-)-1-hydroxy-2-methylpropanephosphonic acid 
• 6738-17-6 (Z)-benzyl N,N'-dicyclohexylcarbamimidate 
• 17176-77-1 Dibenzyl phosphite 
• 78-84-2 isobutyraldehyde 

Downstream Products

• 138643-81-9 (S)-2-tert-Butoxycarbonylamino-3-methyl-butyric acid (S)-1-(bis-benzyloxy-phosphoryl)-2-methyl-propyl ester 
• 138643-80-8 (S)-2-tert-Butoxycarbonylamino-3-methyl-butyric acid (R)-1-(bis-benzyloxy-phosphoryl)-2-methyl-propyl ester 
• 135087-15-9 (S)-2-tert-Butoxycarbonylamino-3-phenyl-propionic acid (S)-1-(bis-benzyloxy-phosphoryl)-2-methyl-propyl ester 
• 135087-16-0 (S)-2-tert-Butoxycarbonylamino-3-phenyl-propionic acid (R)-1-(bis-benzyloxy-phosphoryl)-2-methyl-propyl ester 
• 130769-87-8 2-Benzyloxycarbonylamino-pentanedioic acid 5-[1-(bis-benzyloxy-phosphoryl)-2-methyl-propyl] ester 1-tert-butyl ester 

Relevant academic research and scientific papers

N-Hydroxy-α-amino phosphonate derivatives as potential haptens for eliciting catalytic antibodies

An efficient synthesis of N-hydroxy-α-amino phosphonate derivatives has been developed using a Mitsunobu reaction with N-phenoxycarbonyl-O-tert-butyl-alkoxycarbonyl hydroxylamine and α-hydroxy phosphonates.

A Simple, Efficient Synthesis of Dibenzyl and Di-p-nitrobenzyl 1-Hydroxyalkanephosphonates

Dibenzyl and di-p-nitrobenzyl 1-hydroxyalkanephosphonates 3a-i are prepared by alkylation of 1-hydroxyalkanephosphonic acids 1 with O-benzyl and O-(p-nitrobenzyl)-N,N'-dicyclohexylisoureas 2.