127653-30-9

Upstream product

• 207223-84-5 {4-[(methoxymethoxy)methyl]phenyl}methanol 
• 104292-95-7 methyl 4-<(methoxymethoxy)methyl>benzoate 

Downstream Products

• 127653-39-8 1-(4-Methoxymethoxymethyl-phenyl)-prop-2-yn-1-ol 
• 127653-33-2 1-(2,2-Dibromo-vinyl)-4-methoxymethoxymethyl-benzene 
• 127653-42-3 1,6-Bis-(4-methoxymethoxymethyl-phenyl)-hexa-2,4-diyne-1,6-diol 
• 127653-02-5 C₂₆H₂₂O₄ 
• 127653-01-4 C₂₄H₂₂O₄ 
• 127653-00-3 C₂₂H₂₂O₄ 
• 127653-10-5 {4-[8-(4-Hydroxymethyl-phenyl)-octa-1,3,5,7-tetraynyl]-phenyl}-methanol 
• 127653-09-2 {4-[6-(4-Hydroxymethyl-phenyl)-hexa-1,3,5-triynyl]-phenyl}-methanol 
• 127653-08-1 (4,4'-(buta-1,3-diyne-1,4-diyl)bis(4,1-phenylene))dimethanol 
• 127653-48-9 1-Buta-1,3-diynyl-4-methoxymethoxymethyl-benzene 
• 127653-36-5 1-Ethynyl-4-methoxymethoxymethyl-benzene 
• 127653-18-3 C₂₂H₁₀O₂ 
• 127653-17-2 C₂₀H₁₀O₂ 
• 127653-16-1 4,4'-(buta-1,3-diyne-1,4-diyl)dibenzaldehyde 

Relevant academic research and scientific papers

Nickel-catalyzed intermolecular coupling of 1,3-dienes and aldehydes via transmetalation of nickelacycles with diisobutylaluminum acetylacetonate

Intermolecular coupling reactions of 1,3-dienes and aldehydes via transmetalation of nickelacycle intermediate with iBu2Al-acac were investigated. In the reactions, a linear adduct or a branched adduct was produced, depending upon the nature of 1,3-dienes and aldehydes, via two nickelacycles that were relatively stable among the four possible nickelacycles because of the equilibrium with π-allynickel forms.