514805-23-3

Upstream product

• 64-18-6 formic acid 
• 19718-49-1 4-amino-3-iodobenzoic acid methyl ester 

Downstream Products

• 514805-24-4 4-formylamino-isophthalic acid dimethyl ester 
• 1266610-57-4 C₂₂H₂₃ClINO₅S 
• 1432726-65-2 (E)-methyl 3-iodo-4-[N-(1-p-toluenesulfonyltetradec-2-en-2-yl)formamido]-benzoate 
• 1432726-58-3 (E)-methyl 3-iodo-4-[N-(1-p-toluenesulfonyl)hex-2-en-2-ylformamido]benzoate 
• 1266610-47-2 methyl 2-n-butyl-3-(p-toluenesulfonyl)-1H-indole-5-carboxylate 
• 514805-27-7 4-{Formyl-[(E)-1-(toluene-4-sulfonylmethyl)-but-1-enyl]-amino}-3-iodo-benzoic acid methyl ester 
• 514805-26-6 4-{Formyl-[(E)-1-(toluene-4-sulfonylmethyl)-but-1-enyl]-amino}-isophthalic acid dimethyl ester 
• 514805-29-9 4-{Formyl-[(E)-1-methoxymethyl-2-(toluene-4-sulfonyl)-vinyl]-amino}-isophthalic acid dimethyl ester 

Relevant academic research and scientific papers

Ruthenium-Catalyzed 1,6-Aromatic Enamide-Silylalkyne Cycloisomerization: Approach to 2,3-Disubstituted Indoles

Cycloisomerization is an atom economic procedure that converts dienes and enynes into cyclic molecules. To date, cycloisomerization between enamides and silylalkynes has not been explored. We found that N-acyl-N-vinyl-2-silylalkynylaniline derivatives und

Conjugate additions of o-iodoanilines and methyl anthranilates to acetylenic sulfones. A new route to quinolones including first syntheses of two alkaloids from the medicinal herb Ruta chalepensis

A novel synthesis of 2-substituted 4-quinolones was developed on the basis of the conjugate additions of appropriately ortho-substituted anilines to acetylenic sulfones followed by intramolecular acylation of the corresponding sulfone-stabilized anions. C