924635-55-2

Upstream product

• 534-22-5 2-methylfuran 
• 886493-41-0 7-[hydroxy(phenyl)methyl]-6-(4-methylphenylsulfonamido)-2,3-dihydro-1,4-benzodioxine 
• 164526-10-7 (7-nitro-2,3-dihydro-1,4-benzodioxin-6-yl)-(phenyl)methanone 
• 164526-15-2 (7-amino-2,3-dihydro-1,4-benzodioxin-6-yl)-(phenyl)methanone 
• 93637-87-7 2,3-dihydro-1,4-benzodioxin-6-yl(phenyl)methanone 
• 98-88-4 benzoyl chloride 
• 493-09-4 benzo-1,4-dioxane 
• 886493-75-0 7-benzoyl-6-(4-methylphenylsulfonamido)-2,3-dihydro-1,4-benzodioxine 

Downstream Products

• 1613377-99-3 (3E)-4-[6-(4-methylphenyl)sulfonyl-8-phenyl-2,3-dihydro-6H-[1,4]-dioxino[2,3-f]indol-7-yl]but-3-en-2-one 
• 920481-88-5 4-[6-(4-methylphenylsulfonyl)-8-phenyl-2,3-dihydro-6H-[1,4]dioxino[2,3-f]indol-7-yl]-2-butanone 

Relevant academic research and scientific papers

Oxidative Furan-to-Indole Rearrangement. Synthesis of 2-(2-Acylvinyl)indoles and Flinderole C Analogues

Oxidative rearrangement of 2-(2-aminobenzyl)furans affording 2-(2-acylvinyl)indoles in a stereocontrolled manner in good-to-excellent yields has been developed. Thus, (2-aminobenzyl)furans with electron-releasing alkoxy substituents in the phenyl group fo

Simple route to 3-(2-indolyl)-1-propanones via a furan recyclization reaction

A simple route to 1-R-3-(2-indolyl)-1-propanones has been elaborated based on recyclization of 2-(2-aminobenzyl)furan derivatives. Being a modification of the Reissert indole synthesis, our approach employs the furan ring as a source of carbonyl function. This approach is general and allows varying of substituents in aromatic ring as well as in 3-position of indole nucleus.