57077-15-3

Upstream product

• 408526-05-6 1,1-bis(p-chlorophenyl)-3-phenylpropargyl alcohol 
• 60-29-7 diethyl ether 
• 75-36-5 acetyl chloride 
• 7647-01-0 hydrogenchloride 
• 7664-93-9 sulfuric acid 
• 64-19-7 acetic acid 
• 1004-22-4 (phenylethynyl)sodium 
• 536-74-3 phenylacetylene 
• 2642-81-1 1,1-bis(p-chlorophenyl)ethene 
• 98-88-4 benzoyl chloride 
• 90-98-2 4,4'-Dichlorobenzophenone 

Downstream Products

• 606-86-0 1,3,3-triphenylpropan-1-one 
• 65-85-0 benzoic acid 
• 90-98-2 4,4'-Dichlorobenzophenone 

Relevant academic research and scientific papers

A metal-free tandem dehydrogenative α-arylation reaction of propargylic alcohols with 2-alkynylbenzaldoximes toward the synthesis of α-(4-bromo-isoquinolin-1-yl)-propenone skeletons

A tandem reaction of 2-alkynylbenzaldoximes with propargylic alcohols has been developed for the synthesis of α-(4-bromo-isoquinolin-1-yl)-propenones. Employing 2-alkynylbenzaldoximes as a precursor in the presence of Br2 generates 4-bromo-isoquinoline-N-

Acylation of Alkenes with the Aid of AlCl3 and 2,6-Dibromopyridine

Friedel-Crafts-type acylation of alkenes with acyl chlorides has been successfully conducted with a wide substrate scope by the combined use of AlCl3 and 2,6-dibromopyridine. Trisubstituted alkenes afford allylketones or vinylketones depending on the presence or absence of hydrogen atom(s) at the β-position to the acylation site, while monosubstituted alkenes exclusively afford vinylketones.