82113-06-2

Upstream product

• 82113-04-0 N-hydroxysuccinimide ester of (p-methoxybenzyloxycarbonyl)-α-aminoisobutyryl-L-phenylalanyl-D-prolyl-L-alanine 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 43041-12-9 methyl (2R)-pyrrolidine-2-carboxylate 
• 82113-05-1 N-hydroxysuccinimide ester of L-alanine hydrochloride 
• 82113-03-9 N-(p-methoxybenzyloxycarbonyl)-α-aminoisobutyryl-L-phenylalanyl-D-proline 
• 82113-02-8 N-(p-methoxybenzyloxycarbonyl)-α-aminoisobutyryl-L-phenylalanyl-D-proline methyl ester 
• 183609-55-4 L-phenylalanyl-D-proline methyl ester 
• 77087-63-9 N-(tert-butyloxycarbonyl)-L-phenylalanyl-D-proline methyl ester 
• 77100-17-5 L-phenylalaninyl-L-proline methyl ester hydrochloride 
• 3392-05-0 Boc-Ala-O-N-hydroxysuccinimide 
• 344-25-2 D-Prolin 

Downstream Products

• 71996-70-8 cyclo(α-aminoisobutyryl-L-phenylalanyl-D-prolyl-L-alanyl) 

Relevant academic research and scientific papers

Improved Synthesis of chlamydocin: Cyclization Studies of Tetrapeptides Containing Five α-Substituents

A complete search for the optimal conditions for preparing cycling tetrapeptide 2 was carried out.In this study all four possible sequences of the linear tetrapeptide precursors were synthesized and cyclized.The results establish that one linear sequence is especially favorable for synthesizing the peptide ring system in chlamydocin (1).