122483-60-7

Upstream product

• 872130-35-3 N-benzyloxycarbonyl-L-phenylalanyl-DL-α-acetoxyglycine methyl ester 
• 23828-09-3 N-(benzyloxycarbonyl)-L-phenylalanyl-L-serine methyl ester 
• 188302-22-9 N-benzyloxycarbonyl-L-phenylalanyl-DL-α-(ethylthio)glycine methyl ester 
• 17554-22-2 N-benzyloxycarbonyl-L-phenylalanyl-L-threonine methyl ester 

Downstream Products

• 106872-25-7 2-(2-Benzyloxycarbonylamino-3-phenyl-propionylamino)-but-3-enoic acid methyl ester 
• 708228-79-9 Z-Phe-Gly-OMe 

Relevant academic research and scientific papers

2-Cyclopentadienylglycine, a new α-amino acid and its use for η5-complex formation

The reaction of α-bromohippuric acid methyl ester with nickelocene, cyclopentadienylthallium or cyclopentadienyltrimethylsilane afforded N-benzoyl-2-cyclopentadienylglycine methyl ester (1) as two double bond isomers 1a and 1b. Similarly, the cyclopentadi

Generation of α-Acetoxyglycine Residues within Peptide Chains: A New Strategy for the Modification of Oligopeptides

Seryl and threonyl peptides are converted into α-acetoxyglycyl peptides by treatment with lead tetraacetate.Reaction of these acetoxy derivatives or the more reactive α-chloroglycyl peptides with thiols, dithiols and carbohydrates allows the attachment of

CONVERSION OF SERINE AND THREONINE RESIDUES INTO α-ACYLOXY-, α-ALKYLTHIO-, AND α-HALOGENOGLYCINE MOIETIES: A NEW STRATEGY FOR THE MODIFICATION OF PEPTIDES

Selective modification of serine and threonine containing peptides is accomplished by oxidation with lead tetraacetate.Conversion of the derived α-acetoxyglycine derivative into α-alkylthio- and α-halogenoglycine residues offers a novel synthetic route to