1318261-52-7

Upstream product

• 558-13-4 carbon tetrabromide 
• 99902-03-1 2-(thien-3-yl)benzaldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 

Downstream Products

• 1318261-62-9 4-(4-fluorophenyl)naphtho[2,1-b]thiophene 
• 1318261-60-7 4-(p-tolyl)naphtho[2,1-b]thiophene 
• 1318261-61-8 4-(4-chlorophenyl)naphtho[2,1-b]thiophene 
• 1318261-58-3 4-(4-methoxyphenyl)naphtho[2,1-b]thiophene 
• 1318261-64-1 4-(naphtho[2,1-b]thiophen-4-yl)benzaldehyde 
• 1318261-66-3 4-(4-methyl-3-nitrophenyl)naphtho[2,1-b]thiophene 
• 1318261-68-5 4-(2-(methoxymethyl)phenyl)naphtho[2,1-b]thiophene 
• 1318261-63-0 C₁₉H₁₁NS 
• 1318261-65-2 methyl 4-(naphtho[2,1-b]thiophen-4-yl)benzoate 
• 1318261-59-4 4-phenylnaphtho[2,1-b]thiophene 

Relevant academic research and scientific papers

Exploring the Reactivity of N-Alkynylated Sulfoximines: Acid-Catalyzed Cyclizations

N-Alkynylated sulfoximines undergo acid-promoted cyclization processes under mild reaction conditions. The transformations proceed in short reaction times affording sulfoximidoyl-functionalized naphtho[2,1-b]thiophenes or pyrrolo[1,2-a]quinolines in up to

Synthesis of pyrrolo-/indolo[1,2-a ]quinolines and naphtho[2,1- b ]thiophenes from gem -dibromovinyls and sulphonamides

A highly efficient and simple route for the synthesis of pyrrolo-/indolo[1,2-a]quinolines and naphtho[2,1-b]thiophenes from gem-dibromovinyls and sulphonamides is reported. The noteworthy feature of this report is that the methodology involves a two-step protocol to synthesize tri- and tetracyclic heterocycles in a one-pot fashion through the Cu(I)-catalyzed formation of ynamide followed by a Ag(I)-assisted intramolecular hydroarylation. The photophysical properties of representative examples of pyrrolo- and indolo[1,2-a]quinolines in solid and solution states have also been studied.

Modular synthesis of naphthothiophenes by Pd-catalyzed tandem direct arylation/Suzuki coupling

A short and highly modular three-step synthesis of a new class of substituted naphthothiophenes has been developed exploiting a Pd-catalyzed tandem direct arylation/Suzuki coupling transformation as the key step.