1189760-24-4Relevant academic research and scientific papers
Synthesis of 2′,4-diarylbenzophenones through site-selective suzuki-miyaura reactions of bis(triflates) of 2′,4-dihydroxybenzophenones
Nawaz, Muhammad,Ullah, Ihsan,Abid, Obaid-Ur-Rahman,Villinger, Alexander,Langer, Peter
, p. 6670 - 6684 (2012/01/04)
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
Nawaz, Muhammad,Adeel, Muhammad,Ibad, Muhammad Farooq,Langer, Peter
, p. 2154 - 2156 (2011/04/15)
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.
