摘要

An efficient synthesis of alpha-fluorochalcones (1,3-diphenyl-2-fluoroprop-2-en-1-one) based on the Suzuki-Miyaura palladium-catalyzed cross-coupling reaction of arylboronic acids with alpha-fluorocinnamoyl chlorides in the presence of Cs2CO3 in toluene is described. This approach allows the synthesis of fluorinated analogues of functionalized natural chalcones.

  • 出版日期2013-2-11

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