960159-69-7

Upstream product

• 536-74-3 phenylacetylene 
• 1333773-17-3 2-[4,6-bis(phenylethynyl)-3-(tetrahydro-2H-2-pyranyloxy)phenoxy]tetrahydro-2H-pyran 

Downstream Products

• 24534-44-9 2,6-Diphenylbenzo<1,2-b:5,4-b'>difuran 
• 122118-04-1 2,3,5,6-Tetraphenylbenzo<1,2-b:5,4-b'>difuran 
• 1333773-12-8 3,5-bis(pentafluorophenyl)-2,6-diphenylbenzo[1,2-b:5,4-b']difuran 
• 1333773-20-8 5,5'-bis(pentafluorophenyl)-2,2',6,6'-tetraphenyl-3,3'-bibenzo[1,2-b:5,4-b']difuran 
• 1333773-11-7 3,5-bis[4-(9H-carbazolyl)phenyl]-2,6-diphenylbenzo[1,2-b:5,4-b']difuran 
• 105948-79-6 3,5-bis[4-(N,N-dimethylamino)phenyl]-2,6-diphenylbenzo[1,2-b:5,4-b']difuran 
• 1092578-52-3 3,5-bis[4-(N,N-diphenylamino)phenyl]-2,6-diphenylbenzo[1,2-b:5,4-b']difuran 

Relevant academic research and scientific papers

Modular synthesis and photophysical and electrochemical properties of 2,3,5,6-tetraaryl-substituted benzo[1,2-b:5,4-b′]difurans

We developed a versatile synthesis of tetraaryl-substituted benzo[1,2-b:5,4-b′]difurans (m-BDFs) via a zinc-mediated intramolecular double cyclization reaction of 4,6-bis(phenylethynyl)-1,3-benzenediol, followed by a palladium-catalyzed cross-coupling rea

Double annulations of dihydroxy- and diacetoxy-dialkynylbenzenes. An efficient construction of benzodifurans

An efficient synthetic route to construct disubstituted benzodifurans from dihydroxy- or diacetoxy-dialkynylbenzenes utilizing Cs2CO3 or Pd(OAc)2/Cs2CO3 promoted double annulations is described. The s

Palladium-catalyzed double annulations to construct multisubstituted benzodifurans

(Chemical Equation Presented) Efficient synthetic routes to construct multisubstituted benzo[1,2-b:5,4-b′]difurans and benzo[1,2-b:4,5-b′] difurans from bis(allyloxy)bis(alkynyl)benzenes or bis(alkynyl)dihydroxybenzenes and allylic halides utilizing palla