342416-53-9

Upstream product

• 19615-48-6 5-formyl-2-methyl-furan-3-carboxylic acid ethyl ester 
• 155345-18-9 methyl 1-methoxymethyl-5-tosylmethyl-1H-pyrrole-3-carboxylate 

Downstream Products

• 342416-54-0 methyl 5-[2-(4-ethoxycarbonyl-5-methylfuran-2-yl)-2-oxo-1-tosylethyl]-N-methoxymethylpyrrol-3-carboxylate 
• 342416-55-1 methyl 5-[2-acetoxy-2-(4-ethoxycarbonyl-5-methylfuran-2-yl)-1-tosylethenyl]-N-methoxymethylpyrrol-3-carboxylate 
• 342416-57-3 ethyl 4-acetoxy-2-methyl-8-methoxycarbonyl-5-tosyl-6H-furo[3,2-e]indole-1-carboxylate 
• 342416-56-2 ethyl 4-acetoxy-2-methyl-8-methoxycarbonyl-N-methoxymethyl-5-tosyl-6H-furo[3,2-e]indole-1-carboxylate 

Relevant academic research and scientific papers

Photochemistry of tosylstilbenoids in the preparation of complex heterocyclic compounds. Synthesis of a cyclopropafuroindolone analogue of the DNA-alkylating section of the antitumor compound CC-1065

(equation presented) A novel photocyclization of tosylstilbenoids is used in the preparation of a cyclopropafuroindolone analogue of the DNA-alkylating unit of the antitumor compound CC-1065.