903528-84-7

Upstream product

• 116460-34-5 N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-valyl-L-phenylalanine 
• 903528-94-9 [(S)-1-((S)-1-Chlorocarbonyl-2-phenyl-ethylcarbamoyl)-2-methyl-propyl]-carbamic acid 9H-fluoren-9-ylmethyl ester 

Downstream Products

• 913639-59-5 Fmoc-Val-Phe-ψ(NH-CO-NH)-Ala-Leu-OH 
• 903529-01-1 [(S)-1-((R)-1-Isocyanato-2-phenyl-ethylcarbamoyl)-2-methyl-propyl]-carbamic acid 9H-fluoren-9-ylmethyl ester 

Relevant academic research and scientific papers

An efficient conversion of the carboxylic group of N-Fmoc α-amino acids/peptide acids into N-formamides employing isocyanates as key intermediates

(Chemical Equation Presented) Reaction of 96% formic acid with isocyanates derived from N-Fmoc α-amino acids/peptide acids catalyzed by DMAP has yielded a new class of stable formamides as crystalline solids which have been characterized by IR, 1/su

Nα-Fmoc-peptide azides: Synthesis, isolation, characterization and utility in the extension of peptide chains

Syntheses of Nα-Fmoc-peptide azides employing acid chloride as well as mixed anhydride methods have been carried out. The resulting Fmoc-peptide azides prepared have been isolated as solids in good yield (75-92 %) and are found to be analytical