569672-63-5

Upstream product

• 626-41-5 3,5-dibromophenol 
• 75-77-4 chloro-trimethyl-silane 
• 517895-16-8 1,3-dibromo-5-(hexyloxy)benzene 
• 111-25-1 1-bromo-hexane 

Downstream Products

• 1267662-13-4 C₂₁H₃₇BO₃Si 
• 1267662-14-5 C₄₂H₅₈O₂Si₂ 
• 1267662-15-6 C₃₆H₄₀I₂O₂ 
• 1267662-16-7 C₆₆H₉₀O₄Si₂ 
• 1267662-17-8 C₆₀H₇₂I₂O₄ 
• 569672-55-5 5,5'-bis({3-hexoxy-5-[(triisopropylsilyl)ethynyl]phenyl}ethynyl)-2,2':6',2''-terpyridine 
• 569672-30-6 5,5''-bis[(3-bromo-5-hexoxyphenyl)ethynyl]-2,2':6',2''-terpyridine 
• 517895-32-8 2-bromo-5-{[3-hexoxy-5-({3-hexoxy-5-[(triisopropylsilyl)ethynyl]phenyl}ethynyl)phenyl]ethynyl}pyridine 
• 569672-37-3 1-hexoxy-3-({3-hexoxy-5-[(trimethylsilyl)ethynyl]phenyl}ethynyl)-5-[(triisopropylsilyl)ethynyl]benzene 
• 517895-28-2 1-hexoxy-3-[1-(3-hexoxy-5-ethynylphenyl)ethynyl]-5-[(triisopropylsilyl)ethynyl]benzene 
• 569672-52-2 2-bromo-5-({3-hexoxy-5-[(triisopropylsilyl)ethynyl]phenyl}ethynyl)pyridine 
• 569672-66-8 1-hexyloxy-3-[(triisopropylsilyl)ethynyl]-5-[(trimethylsilyl)ethynyl]benzene 
• 517895-25-9 1-ethynyl-3-(hexyloxy)-5-[(triisopropylsilyl)ethynyl]benzene 
• 569672-65-7 1-bromo-3-hexoxy-5-[(triisopropylsilyl)ethynyl]benzene 

Relevant academic research and scientific papers

Synthesis of shape-persistent macrocycles by a one-pot suzuki-miyaura cross-coupling reaction

Ring creation: Shape-persistent macrocyclic structures were prepared by a one-pot catalyst-transfer Suzuki-Miyaura cross-coupling (CTSMCC) reaction (see figure). The reaction of 3,6-dibromo-substituted carbazoles and diboronic ester monomers afforded shap

Shape-persistant macrocycles with terpyridine units: Synthesis, characterization, and structure in the crystal

The synthesis of a variety of shape-persistent macrocycles with either one (1a-d, 2) or two (opposing) terpyridine units (3, 4, 5a-c) and inner diameters of up to 2 nm is described. The sequences are mainly based on transition metal cross-coupling reactio