160617-39-0

Upstream product

• 63649-15-0 L-phenylalanyl-L-leucine benzyl ester 
• 103321-49-9 9H-fluoren-9-ylmethyl (2-chloro-2-oxoethyl)carbamate 
• 29022-11-5 N-(fluoren-9-ylmethoxycarbonyl)glycine 
• 35661-40-6 N-Fmoc L-Phe 
• 1738-69-8 L-Leucine benzyl ester 
• 103321-61-5 Fmoc-Phe-Leu-OBzl 
• 103321-57-9 2S-flouren-9-ylmethoxycarbonylamino-3-phenylpropionyl chloride 
• 117370-45-3 (9-fluorenylmethyloxycarbonyl)glycyl-L-phenylalanine 
• 903528-95-0 [(1-chlorocarbonyl-2-phenyl-ethylcarbamoyl)-methyl]-carbamic acid 9H-fluoren-9-ylmethyl ester 
• 903528-85-8 Fmoc-Gly-Phe-N₃ 

Downstream Products

• 69729-07-3 H-Gly-Gly-Phe-Leu-OBzl 
• 124482-87-7 Fmoc-Gly-Gly-Phe-Leu-OBzl 
• 88099-29-0 Fmoc-Tyr(Bzl)-Gly-Gly-Phe-Leu-OBzl 
• 100930-01-6 Tyr-Gly-Gly-Phe-Leu formate 
• 73994-89-5 (S)-benzyl 2-((S)-2-(2-aminoacetamido)-3-phenylpropanamido)-4-methylpentanoate 

Relevant academic research and scientific papers

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

Synthesis of [Leu5]enkephalin using Fmoc-Amino Acid Chlorides/KOAt

The coupling of Fmoc-amino acid chlorides can be mediated by the potassium salt of 1-hydroxy-7-azabenzotriazole. Thus the synthesis of [Leu5]enkephalin has been accomplished in good yield and purity.

((9-Fluorenylmethyl)oxy)carbonyl (Fmoc) Amino Acid Chlorides. Synthesis, Characterization, and Application to the Rapid Synthesis of Short Peptide Segments

Fmoc amino acid chlorides are described as stable, easily synthesized coupling agents and shown to be useful in a novel method of rapid, repetitive peptide synthesis