486403-27-4

Upstream product

• 486403-21-8 (S)-2-{20-[(R)-1-Hydroxymethyl-2-(4-methoxy-benzyloxy)-ethoxy]-icosa-9,11-diynyloxy}-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 482620-96-2 1-((S)-2-Dec-9-ynyloxy-3-trityloxy-propoxymethyl)-4-methoxy-benzene 
• 482621-01-2 1-((R)-2-Dec-9-ynyloxy-3-trityloxy-propoxymethyl)-4-methoxy-benzene 
• 482621-00-1 (R)-1-(4-Methoxy-benzyloxy)-3-trityloxy-propan-2-ol 
• 482620-97-3 (R)-2-Dec-9-ynyloxy-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 119227-71-3 9-decynyl mesylate 
• 220641-23-6 1-O-(triphenylmethyl)-3-O-(4'-methoxybenzyl)-sn-glycerol 
• 824-94-2 p-methoxybenzyl chloride 
• 109786-76-7 (R)-4-(((4-methoxybenzyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolane 
• 109786-77-8 (S)-3-((4-methoxybenzyl)oxy)propane-1,2-diol 
• 486403-24-1 C₆₂H₉₄O₈ 

Relevant academic research and scientific papers

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.