482620-96-2

Upstream product

• 220641-23-6 1-O-(triphenylmethyl)-3-O-(4'-methoxybenzyl)-sn-glycerol 
• 119227-71-3 9-decynyl mesylate 
• 824-94-2 p-methoxybenzyl chloride 
• 109786-73-4 (S)-4-[(4-methoxybenzyloxy)methyl]-2,2-dimethyl-1,3-dioxolane 
• 109786-74-5 (R)-3-(4-methoxybenzyloxy)propane-1,2-diol 

Downstream Products

• 609848-15-9 C₈₄H₁₀₄O₆ 
• 609848-13-7 C₈₄H₁₀₆O₆ 
• 482621-06-7 C₇₃H₉₈O₇ 
• 482621-12-5 C₇₃H₉₈O₇ 
• 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 
• 482621-16-9 1-{(R)-3-Dec-9-ynyloxy-2-[20-((R)-2-dec-9-ynyloxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-propoxymethyl}-4-methoxy-benzene 
• 486403-08-1 C₆₂H₉₂O₈ 
• 486403-27-4 C₆₂H₉₂O₈ 
• 609848-05-7 C₆₂H₉₄O₈ 
• 486403-24-1 C₆₂H₉₄O₈ 
• 609848-11-5 (S)-2-[20-((S)-1-Hydroxymethyl-2-trityloxy-ethoxy)-icosa-9,11-diynyloxy]-3-trityloxy-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 
• 482621-05-6 (R)-2-[20-((R)-2-Hydroxy-3-trityloxy-propoxy)-icosa-9,11-diynyloxy]-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 609848-04-6 (R)-2-{20-[(R)-1-Hydroxymethyl-2-(4-methoxy-benzyloxy)-ethoxy]-icosa-9,11-diynyloxy}-3-(4-methoxy-benzyloxy)-propan-1-ol 

Relevant academic research and scientific papers

Design, synthesis, and self-assembly of an ether and amide linkage-based cyclic lipid

A novel 48-membered cyclic lipid, in which two ether and two amide groups serve as a linker between its hydrophilic and hydrophobic moiety, was synthesized starting from d-1,2-O-isopropylidene-sn-glycerol. The synthetic scheme is featured by the selective

Efficient synthesis of parallel cyclobolaphiles having two diacetylenes: Mimetics of archaeal membrane lipids

Chiral 48-membered parallel cyclobolaphiles and their diastereomer having two diacetylenes were efficiently synthesized by utilizing both the selective deprotection and the cross-coupling method of two distinct acetylenic compounds.

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.