87241-87-0Relevant academic research and scientific papers
Optimized palladium(0)-catalyzed Suzuki cross-coupling reaction of polystyrene-supported selenenyl flavanones: A convenient preparation of biaryl-chromen-4-one
Tang,Li, Wen,Gao, Zhangyong,Zhang, Lianpeng,Ma, Qiushi
experimental part, p. 585 - 589 (2012/05/19)
Application of the Suzuki cross-coupling reaction for efficient synthesis of diverse substituted biaryl-chromen-4-ones using an optimized palladium(0) catalyst system is reported. The coupling of arylboronic acids with the resin-bound bromoflavanones whic
Microwave enhanced palladium catalysed coupling reactions: A diversity-oriented synthesis approach to functionalised flavones
Fitzmaurice, Richard J.,Etheridge, Zac C.,Jumel, Emelie,Woolfson, Derek N.,Caddick, Stephen
, p. 4814 - 4816 (2007/10/03)
Microwave enhanced diversity-oriented synthesis (MEDOS) using palladium catalysed protocols is introduced as a powerful new strategy for the synthesis of systematically modified small molecules and is highlighted by application to functionalised flavones. The Royal Society of Chemistry 2006.
SYNTHESIS OF 6- AND 8-PHENYL-SUBSTITUTED FLAVONOIDS.
Matsumura,Tsuchiya,Takeda,Imafuku
, p. 2037 - 2043 (2007/10/02)
3-Acetylbiphenyl-4-ol and -2-ol were condensed with substituted benzaldehydes to give respectively 5 prime - and 3 prime -phenyl-substituted chalcones which were cyclized to afford 6- and 8-phenylflavanones. The chalcones also gave the corresponding 6- an
