1189760-30-2

Upstream product

• 17422-74-1 3-Formylchromone 
• 1189760-11-9 methyl 2-(trifluoromethanesulfonyloxy)-5-[2-(trifluoromethanesulfonyloxy)benzoyl]benzoate 
• 172975-69-8 3,5-dimethylphenyl boronic acid 
• 1189760-22-2 methyl 3',5'-dimethyl-4-[2-(trifluoromethanesulfonyloxy)benzoyl]biphenyl-2-carboxylate 
• 2156-04-9 4-Vinylphenylboronic acid 

Relevant academic research and scientific papers

Synthesis of 2′,4-diarylbenzophenones through site-selective suzuki-miyaura reactions of bis(triflates) of 2′,4-dihydroxybenzophenones

Palladium(0)-catalyzed Suzuki cross-coupling reactions of the bis(triflates) of 2′,4-dihydroxybenzophenones afforded 2′,4-diarylbenzophenones. The reactions proceeded with very good site selectivity in favour of the 4-position. Palladium(0)-catalyzed Suzuki cross-coupling reactions of the bis(triflates) of 2′,4- dihydroxybenzophenones afforded 2′,4-diarylbenzophenones. The reactions proceeded with very good site selectivity infavour of the 4-position. Copyright

Synthesis of functionalized 2′,4-diarylbenzophenones based on site-selective Suzuki cross-coupling reactions

The palladium(0)-catalyzed Suzuki cross-coupling reaction of the bis(triflates) of 2′,4-dihydroxybenzophenones afforded 2′,4-diarylbenzophenones. The reactions proceeded with very good site selectivity. The first attack occurred at carbon atom C-4. Georg Thieme Verlag Stuttgart.