540803-89-2

Upstream product

• 1239867-66-3 3-methylbut-2-en-1-yl 2-(2-iodophenyl)-N-phenylacetimidate 
• 62300-07-6 o-iodophenylacetyl chloride 
• 62-53-3 aniline 
• 18698-96-9 o-iodophenylacetic acid 

Downstream Products

• 540804-09-9 2-(2-hex-1-ynylphenyl)-N-phenylacetamide 
• 1301714-59-9 2-(2-ethynylphenyl)-N-phenylacetamide 
• 1301714-75-9 4-methyl-2-(2-(2-oxo-2-(phenylamino)ethyl)phenyl)-N-phenyl-1-naphthamide 
• 20011-90-9 5H,7H-dibenzo[b,d]azepin-6-one 
• 1379820-93-5 2-([1,1'-biphenyl]-2-yl)-N-phenylacetamide 
• 4494-54-6 N-phenylhomophthalimide 
• 540803-96-1 2-(2-hex-1-ynylphenyl)-N-phenylthioacetamide 

Relevant academic research and scientific papers

Synthesis of 2-phenylnaphthalenes through gold-catalyzed dimerization via a highly selective carbon nucleophile pathway

A protocol for the facile synthesis of 2-phenylnaphthalene has been developed. The benzyl carbon acts as a nucleophilic center in the presence of the amide nitrogen and acetate oxygen, affording the selective formation of a naphthalene scaffold through th

Branch-selective synthesis of oxindole and indene scaffolds: Transition metal-controlled intramolecular aryl amidation leading to C3 reverse-prenylated oxindoles

In an effort to access biologically important scaffolds, a concise branch-selective synthesis of C3 tertiary oxindoles by Cu(I)-catalyzed aryl amidation and 2,2-dimethyl indene by Pd(0)-catalyzed Heck cyclization has been accomplished from acyclic reverse-prenylated intermediates. Oxindole C3-enolate generation using NaH followed by alkylation in the presence of appropriate electrophiles provides a novel route to quaternary C3 reverse-prenylated oxindoles.