125372-58-9

Upstream product

• 125372-52-3 C₂₄H₃₄O₁₀S₂ 
• 125372-56-7 (5S,6S)-1,10-dibenzyloxy-5,6-dimethoxy-3,8-dioxadecane 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 125372-57-8 (5S,6S)-5,6-dimethoxy-1,10-dimercapto-3,8-dioxadecane 

Downstream Products

• 118404-12-9 (S)-2-Amino-thiopropionic acid S-(2-{(2S,3S)-4-[2-(2-benzyloxycarbonylamino-acetylsulfanyl)-ethoxy]-2,3-dimethoxy-butoxy}-ethyl) ester; hydrochloride 
• 118404-14-1 (+)-(5S,6S)-5,6-dimethoxy-S-(N-carbobenzyloxyglycyl-L-alanyl)-1,10-dimercapto-3,8-dioxadecane 
• 125372-59-0 (+)-(5S,6S)-5,6-dimethoxy-S-(N-carbobenzyloxyglycyl)-S'-(N-carbo-tert-butoxy-L-alanyl)-1,10-dimercapto-3,8-dioxadecane 

Relevant academic research and scientific papers

Biomimetic studies using artificial systems. IV. Biomimetic peptide synthesis by using multifunctionalized crown ethers as a novel enzyme model. A new concept in mimicking of enzyme-catalyzed bond-forming reactions.

A novel approach to the mimicking of enzyme-catalyzed bond-forming reactions has been examined using multifunctionalized chiral crown ethers. In addition to the 18-crown-6 moiety as a binding site, the host have one thiol and one thio ester with an N-prot