69604-81-5

Upstream product

• 69604-83-7 N-Formyl-L-alanine benzyl ester 
• 100-51-6 benzyl alcohol 

Downstream Products

• 64818-04-8 2-isocyano-propionic acid benzyl ester 
• 1158966-34-7 C₃₄H₃₄N₂O₇S 
• 1158966-31-4 C₃₁H₃₂N₂O₅S 
• 1158966-35-8 C₃₉H₄₀N₂O₆S 
• 1258863-50-1 C₁₁H₁₁NO₂Se 
• 1258863-64-7 C₂₁H₂₄N₂O₄Se 
• 1303516-15-5 benzyl (S)-2-((S)-2-((S)-2-azido-N-formyl-4-methylpentanamido)-N-formyl-4-methylpentanamido)propanoate 
• 1303516-13-3 benzyl (S)-2-((S)-2-((S)-2-azido-N-formyl-3-methylbutanamido)-N-formyl-4-methylpentanamido)propanoate 

Relevant academic research and scientific papers

Isoselenocyanates derived from amino acid esters: An expedient synthesis and application to the assembly of selenoureidopeptidomimetics, unsymmetrical Selenoureas and selenohydantoins

An important class of organoselenium compounds-α-isoselenocyanato esters 4 hasbeen prepared by a reaction of α-isocyano esters with elemental selenium powder. The reaction issimple, rapid and all the isoselenocyanates havebeen isolated as stable ones after chromatographic purification. These hitherto unreported classes of molecules would be useful building blocks for the preparation of variety of selenium containing peptidomimetics. In this study, the utility of the title molecules in the preparation of selenoureidopeptidomimetics 6, unsymmetrical selenoureas 8 and selenohydantoins 10 isdemonstrated.

On the preparation of enantiomerically pure isonitriles from amino acid esters and peptides

An improved method for the synthesis of enantiomerically pure isonitriles from amino acid esters and dipeptides is described.