28051-16-3

Upstream product

• 81-54-9 1,2,4-trihydroxy-9,10-anthraquinone 
• 1297598-99-2 1,2,4-tris[(trifluoromethylsulfonyl)oxy]anthraquinone 
• 98-80-6 phenylboronic acid 
• 27258-80-6 1,1'-(1,2-phenylene)bis(3-phenyl-2-propyn-1-one) 
• 536-74-3 phenylacetylene 

Relevant academic research and scientific papers

Site-selective arylation of alizarin and purpurin based on Suzuki-Miyaura cross-coupling reactions

A variety of arylated anthraquinones were prepared by site-selective Suzuki-Miyaura cross-coupling reactions of the bis- and tris(triflates) of alizarin and purpurin, respectively. The site-selectivity is controlled by the electronic influence of the carb

Catalytic [2 + 2 + 2] and thermal [4 + 2] cycloaddition of 1,2-bis(arylpropiolyl)benzenes

We have determined that a cationic rhodium(I)/Segphos complex catalyzes an enantio- and diastereoselective intermolecular [2 + 2 + 2] cycloaddition of 1,2-bis(arylpropiolyl)benzenes with various monoalkynes at room temperature to give axially chiral 1,4-t