147377-76-2

Upstream product

• 87-41-2 2-benzofuran-1(3H)-one 
• 147377-67-1 (E)-ethyl 3-(2-(hydroxymethyl)phenyl)acrylate 
• 147377-68-2 ethyl (2-tert-butyldimethylsilyloxymethyl)cinnamate 
• 26260-02-6 2-iodobenzaldehyde 
• 147377-69-3 ethyl 3-(2-tert-butyldimethylsilyloxymethylphenyl)propionate 
• 147377-71-7 3-(2-tert-butyldimethylsilyloxymethylphenyl)propionaldehyde ethylene acetal 
• 147377-70-6 3-(2-tert-butyldimethylsilyloxymethylphenyl)propanal 
• 147377-94-4 3-(2-hydroxymethylphenyl)propionaldehyde ethylene acetal 

Downstream Products

• 147377-83-1 (E)-3-<2-(2-formylethyl)phenyl>-2-methylprop-2-en-1-ol 
• 147377-80-8 (E)-3-<2-<2-(1,3-dioxolan-2-yl)ethyl>phenyl>-2-methylprop-2-en-1-ol 
• 1447254-63-8 2-[2-(1,3-dioxolan-2-yl)ethyl]-N-phenethylbenzimidoyl cyanide 
• 147377-73-9 ethyl (E)-3-<2-<2-(1,3-dioxolan-2-yl)ethyl>phenyl>-2-methylprop-2-enoate 

Relevant academic research and scientific papers

Nickel-catalyzed cross-coupling of alkyl zinc halides for the formation of C(sp2)-C(sp3) bonds: Scope and mechanism

Optimal conditions for a general Ni-catalysed Negishi cross-coupling of alkyl zinc halides with aryl, heteroaryl and alkenyl halides have been determined. These conditions allow the reaction to take place smoothly, with low catalyst loading, and in the pr

A General Synthetic Route to Fused Furans. Total Synthesis of (+)-Pallescensin A

A general and facile synthetic route to fused furans has been developed.The key step of the transformation involves the intramolecular dipolar cycloaddition reaction of the nitrile oxides, 2 and 2', which were generated in situ from the correspondin