119552-93-1

Upstream product

• 119012-04-3 Leu(OH)P 
• 6738-17-6 (Z)-benzyl N,N'-dicyclohexylcarbamimidate 
• 17176-77-1 Dibenzyl phosphite 
• 590-86-3 isovaleraldehyde 
• 6738-17-6 O-benzyl-N,N'-dicyclohexylisourea 
• 130834-65-0 benzyl hydrogen 1-hydroxy-3-methylbutanephosphonate 
• 119552-93-1 dibenzyl 1-hydroxy-3-methylbutanephosphonate 
• 130834-65-0 benzyl hydrogen 1-hydroxy-3-methylbutanephosphonate 

Downstream Products

• 130834-73-0 (S)-2-tert-Butoxycarbonylamino-3-methyl-butyric acid (R)-1-(bis-benzyloxy-phosphoryl)-3-methyl-butyl ester 
• 130834-77-4 (S)-2-tert-Butoxycarbonylamino-3-methyl-butyric acid (S)-1-(bis-benzyloxy-phosphoryl)-3-methyl-butyl ester 
• 135087-14-8 (S)-2-tert-Butoxycarbonylamino-4-methyl-pentanoic acid (R)-1-(bis-benzyloxy-phosphoryl)-3-methyl-butyl ester 
• 135087-13-7 (S)-2-tert-Butoxycarbonylamino-4-methyl-pentanoic acid (S)-1-(bis-benzyloxy-phosphoryl)-3-methyl-butyl ester 
• 1027188-62-0 Trifluoro-methanesulfonic acid 1-(bis-benzyloxy-phosphoryl)-3-methyl-butyl ester 
• 130834-73-0 2-tert-Butoxycarbonylamino-3-methyl-butyric acid 1-(bis-benzyloxy-phosphoryl)-3-methyl-butyl ester 
• 130834-72-9 2-tert-Butoxycarbonylamino-3-phenyl-propionic acid 1-(bis-benzyloxy-phosphoryl)-3-methyl-butyl ester 
• 130834-65-0 benzyl hydrogen 1-hydroxy-3-methylbutanephosphonate 
• 182497-94-5 C₃₁H₃₈NO₈P 
• 130834-74-1 2-Amino-3-phenyl-propionic acid 3-methyl-1-phosphono-butyl ester 
• 130834-65-0 benzyl hydrogen 1-hydroxy-3-methylbutanephosphonate 
• 130834-65-0 benzyl hydrogen 1-hydroxy-3-methylbutanephosphonate 
• 119552-93-1 (-)-1-hydroxyisobutylphosphonic acid dibenzylester 
• 130769-89-0 2-Benzyloxycarbonylamino-pentanedioic acid 1-benzyl ester 5-[1-(bis-benzyloxy-phosphoryl)-3-methyl-butyl] ester 

Relevant academic research and scientific papers

Nafion-supported oxovanadium-catalyzed hydrophosphonylation of aldehydes under solventless conditions

A Nafion resin-supported oxovanadium(IV) catalyst was readily prepared via ion-exchange method. This solid vanadyl perfluorinated sulfonate catalyst was used as an efficient and recoverable catalyst for the hydrophosphonylation of various aldehydes under solventless conditions at room temperature. The catalyst could be recovered by simple filtration and reused without a significant loss of activity.

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.

Synthesis of Novel N-Phosphonoalkyl Dipeptide Inhibitors of Human Collagenase

The synthesis of a series of N-phosphonoalkyl dipeptides 6 is described.Syntheses were devised that allowed the preparation of single diastereoisomers and the assignment of stereochemistry.The compounds were evaluated in vitro for their ability to inhibit

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.