20967-95-7

Upstream product

• 109-77-3 malononitrile 
• 217813-03-1 3-methoxy-2-(trimethylsilyl)phenyl-trifluoromethanesulfonate 
• 2845-89-8 1-chloro-3-methoxy-benzene 
• 372-09-8 cyanoacetic acid 
• 1071-36-9 sodium cyanoacetate 
• 113260-28-9 bis(3-methoxyphenyl)<(trimethylsily)oxy>acetonitrile 
• 591-31-1 3-methoxy-benzaldehyde 
• 112895-90-6 cyanobis(3-methoxyphenyl)methanol 
• 55360-45-7 bis(3-methoxyphenyl)methanol 
• 39193-85-6 3,3'-dimethoxybenzophenone 
• 2398-37-0 3-methoxyphenyl bromide 
• 112895-91-7 chlorobis(3-methoxyphenyl)acetonitrile 
• 7677-24-9 trimethylsilyl cyanide 
• 112895-92-8 chlorobis(3-methoxyphenyl)methane 

Downstream Products

• 112895-95-1 N-(tert-butyloxycarbonyl)-2,2-bis(3-methoxyphenyl)ethylamine 
• 112895-97-3 N-(tert-butyloxycarbonyl)-6-methoxy-4-(3-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline 
• 112895-96-2 N-(tert-butyloxycarbonyl)-N-(hydroxymethyl)-2,2-bis(3-methoxyphenyl)ethylamine 
• 112895-98-4 6-Methoxy-4-(3-methoxy-phenyl)-1,2,3,4-tetrahydro-isoquinoline 
• 112896-00-1 (-)-N-acetyl-6-hydroxy-4-(3-hydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline 
• 112895-99-5 (-)-N-acetyl-6-methoxy-4-(3-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline 
• 112896-01-2 (-)-N-acetyl-6-(4-chlorobutoxy)-4-<3-(4-chlorobutoxy)phenyl>-1,2,3,4-tetrahydroisoquinoline 
• 112965-88-5 (-)-6-methoxy-4-(3-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline 
• 1582779-57-4 2,2-bis(3-methoxyphenyl)hex-5-en-1-amine 
• 112895-98-4 6-Methoxy-4-(3-methoxy-phenyl)-1,2,3,4-tetrahydro-isoquinoline 
• 112896-01-2 1-{6-(4-Chloro-butoxy)-4-[3-(4-chloro-butoxy)-phenyl]-3,4-dihydro-1H-isoquinolin-2-yl}-ethanone 
• 112895-99-5 1-[(R)-6-Methoxy-4-(3-methoxy-phenyl)-3,4-dihydro-1H-isoquinolin-2-yl]-ethanone 
• 112896-00-1 1-[(R)-6-Hydroxy-4-(3-hydroxy-phenyl)-3,4-dihydro-1H-isoquinolin-2-yl]-ethanone 
• 112895-94-0 2,2-bis(3-methoxyphenyl)ethylamine 

Relevant academic research and scientific papers

Palladium-catalyzed decarboxylative arylation of potassium cyanoacetate: Synthesis of α-diaryl nitriles from aryl halides

A palladium-catalyzed decarboxylative coupling of potassium cyanoacetate with aryl bromides and chlorides is described. The reaction conditions feature the absence of additional strong inorganic bases and provide ester functional group tolerance. With Pd(

Straightforward construction of diarylmethane skeletons via aryne insertion into carbon-carbon σ-bonds

Two molar amounts of arynes were found to couple with nitriles via carbon-carbon σ-bond cleavage, assembling diverse diarylmethane skeletons in a straightforward manner. The Royal Society of Chemistry.

A Novel Optically Active Host: Design, Computer Graphics, Synthesis, and Diastereomeric Complex Formation in Aqueous Solution

The application of molecular mechanism (MM2) to the design of the novel optically active macrocyclic host (+)-10 is described.The cavity binding site of host (+)-10 is shaped by both a diphenylmethane and a 4-phenyl-1,2,3,4-tetrahydroisoquinoline unit bri