925900-75-0

Upstream product

• 19514-91-1 4,6-diiodobenzene-1,3-diol 
• 693-02-7 hex-1-yne 
• 854538-41-3 1,5-diacetoxy-2,4-diiodobenzene 
• 925900-90-9 2,4-bis(hex-1'-ynyl)-1,5-diacetoxybenzene 

Downstream Products

• 925900-76-1 1,5-bis(allyloxy)-2,4-bis(hex-1'-ynyl)benzene 
• 925900-78-3 1-allyloxy-5-(but-3'-enyloxy)-2,4-bis(hex-1'-ynyl)benzene 
• 925900-85-2 1,5-bis(but-3'-enyloxy)-2,4-di(hex-1'-ynyl)benzene 
• 925900-77-2 5-(but-3'-enyloxy)-2,4-bis(hex-1'-ynyl)phenol 

Relevant academic research and scientific papers

An efficient synthesis of fused tricycles with a benzene core via intramolecular double ring-closing enyne metathesis

A double enyne metathesis reaction has been developed for the efficient synthesis of tricyclic products with a benzene core in good yields. By this protocol, bisannulated benzenes with different ring sizes may be simultaneously constructed from the corres

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