125372-51-2

Upstream product

• 4981-83-3 2-(Benzyloxy)ethyl p-toluenesulfonate 
• 58841-52-4 2-(benzyloxy)ethyl methanesulfonate 
• 474334-02-6 (4S,5S)-4,5-bis{[2-(benzyloxy)ethoxy]methyl}-2,2-dimethyl-1,3-dioxolane 

Downstream Products

• 474334-04-8 C₂₂H₂₈N₆O₄ 
• 474334-03-7 Methanesulfonic acid (1S,2S)-3-(2-benzyloxy-ethoxy)-1-(2-benzyloxy-ethoxymethyl)-2-methanesulfonyloxy-propyl ester 
• 125372-56-7 (5S,6S)-1,10-dibenzyloxy-5,6-dimethoxy-3,8-dioxadecane 

Relevant academic research and scientific papers

Asymmetric synthesis of novel C2-symmetric bimorpholines

Novel heterocycles - (2S,2′S)-bimorpholine 1 and (3S,3′S)-bimorpholine 2 - were synthesised in >98% e.e. starting from tartaric acid ester.

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