61465-69-8

Upstream product

• 1261486-31-0 Fmoc-Leu-Phe-O-t-Bu 
• 16874-17-2 L-phenylalanine tert-butyl ester 
• 61445-16-7 N-(2-Bromethoxycarbonyl)-leucin 
• 61-90-5 L-leucine 
• 81578-27-0 (S)-2-[(S)-2-([1,3]Dithian-2-ylmethoxycarbonylamino)-4-methyl-pentanoylamino]-3-phenyl-propionic acid tert-butyl ester 

Downstream Products

• 81578-35-0 1,3-Dithian-2-ylmethoxycarbonyl-L-leucyl-L-leucyl-L-phenylalanin-tert-butylester 
• 1261486-35-4 Boc-Phe-Leu-Phe-O-t-Bu 
• 1261486-37-6 Boc-Phe-Leu-Phe-Leu-Phe-O-t-Bu 
• 81578-38-3 1,3-Dithian-2-ylmethoxycarbonyl-l-prolyl-L-valyl-L-phenylalanyl-L-leucyl-L-leucyl-L-phenylalanin-tert-butylester 
• 81578-36-1 L-Leucyl-L-leucyl-L-phenylalanin-tert-butylester 

Relevant academic research and scientific papers

Fully enzymatic peptide synthesis using C-terminal tert-butyl ester interconversion

Chemoenzymatic peptide synthesis is potentially the most cost-efficient technology for the synthesis of short and medium-sized peptides with some important advantages. For instance, stoichiometric amounts of expensive coupling reagents are not required an

The 1,3-Dithian-2-ylmethoxycarbonyl (Dmoc) Group as Two-Step Amino Protective Function in Peptide Chemistry

The 1,3-dithian-2-ylmethoxycarbonyl (Dmoc) group (4) as amino protective function is stable against bases and trifluoroacetic acid.The peptide condensation of Dmoc-amino acids is carried out applying the mixed anhydride or modified carbodiimide procedures