1370552-80-9

Upstream product

• 1337541-80-6 ethyl (4-(hex-1-yn-1-yl)phenyl)carbamate 
• 1337541-83-9 (E)-1-(4-((ethoxycarbonyl)amino)phenyl)-2-iodohex-1-en-1-yl acetate 
• 766-97-2 4-n-methylphenylacetylene 

Downstream Products

• 1370552-58-1 ethyl (4-(3-butyl-4-iodo-5-(p-tolyl)furan-2-yl)phenyl)carbamate 

Relevant academic research and scientific papers

Multisubstituted furan formation from (Z)- or (E)-enynyl acetates: Tandem reactions accelerated by electron-donating groups on aromatic rings

Multisubstituted furans were readily prepared from (Z)- or (E)-conjugated enynyl acetates with NXS under metal-free conditions at room temperature via the same haloallenyl ketone intermediates. This tandem haloallenyl ketone formation-furan formation reaction sequence was accelerated by electron-donating groups on the aromatic rings.