482621-08-9

Upstream product

• 109786-77-8 (S)-3-((4-methoxybenzyl)oxy)propane-1,2-diol 
• 482621-01-2 1-((R)-2-Dec-9-ynyloxy-3-trityloxy-propoxymethyl)-4-methoxy-benzene 
• 482620-98-4 (S)-1-Dec-9-ynyloxy-3-trityloxy-propan-2-ol 
• 482621-00-1 (R)-1-(4-Methoxy-benzyloxy)-3-trityloxy-propan-2-ol 
• 482621-14-7 (R)-3-Dec-9-ynyloxy-propane-1,2-diol 
• 119227-71-3 9-decynyl mesylate 
• 824-94-2 p-methoxybenzyl chloride 
• 109786-76-7 (R)-4-(((4-methoxybenzyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolane 
• 76-83-5 trityl chloride 
• 482621-02-3 (S)-2-Dec-9-ynyloxy-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 482620-99-5 (S)-1-(10-Iodo-dec-9-ynyloxy)-3-trityloxy-propan-2-ol 

Downstream Products

• 482621-09-0 C₇₃H₉₈O₇ 
• 482621-17-0 1-{(S)-3-Dec-9-ynyloxy-2-[20-((S)-2-dec-9-ynyloxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-propoxymethyl}-4-methoxy-benzene 

Relevant academic research and scientific papers

Convergent synthesis of antiparallel cyclobolaphiles having two diacetylenes: Mimetics of membrane components that are found in archaea

Chiral 48-membered antiparallel cyclobolaphiles and their diastereomer having two diacetylenes were convergently synthesized utilizing both cross-coupling method (Cul, pyrrolidine) and Glaser intramolecular cyclization, starting from commercially available D- and L-1, 2-O-isopropylidene-sn-glycerol as chiral sources.