482620-98-4

Upstream product

• 76-83-5 trityl chloride 
• 482621-14-7 (R)-3-Dec-9-ynyloxy-propane-1,2-diol 
• 119227-71-3 9-decynyl mesylate 

Downstream Products

• 482621-09-0 C₇₃H₉₈O₇ 
• 482621-12-5 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 
• 482621-19-2 1-{(R)-3-Dec-9-ynyloxy-2-[20-((S)-2-dec-9-ynyloxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-propoxymethyl}-4-methoxy-benzene 
• 482621-08-9 (S)-2-[20-((S)-2-Hydroxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 482621-11-4 (R)-2-[20-((S)-2-Hydroxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 482620-99-5 (S)-1-(10-Iodo-dec-9-ynyloxy)-3-trityloxy-propan-2-ol 

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.