145193-44-8Relevant academic research and scientific papers
Palladium-catalyzed arylation of cyclopentadienes
Dyker, Gerald,Heiermann, Joerg,Miura, Masahiro,Inoh, Jun-Ichi,Pivsa-Art, Sommai,Satoh, Tetsuya,Nomura, Masakatsu
, p. 3426 - 3433 (2007/10/03)
Cyclopentadiene and metallocenes, typically zirconocene dichloride, are suitable substrates for multiple arylations with aryl bromides in palladium-catalyzed reactions. Thus, various aryl bromides bearing either an electron-donating or an electron-withdrawing substituent can react with these substrates to afford the corresponding 1,2,3,4,5-pentaaryl-1,3-cyclopentadienes in a single preparative step. Derivatives of cyclopentadiene, including di- and trisubstituted cyclopentadienes, and indene are arylated in a similar fashion.
1--(4,1-phenylene)-alkanones and -benzoic Acid Pentaalkyl Esters and their Sodium- and Thallium(I) Complexes
Schumann, Herbert,Kucht, Homa,Kucht, Andreas
, p. 1281 - 1289 (2007/10/02)
Pentaphenylcyclopentadiene (1) reacts with acyl chlorides RC(O)Cl (R = CH3, C3H7, C5H11, C7H15) with formation of the corresponding (1,4-phenylene) alkanones C5H(C6H4C(O)R-4)5 (2a, 2c, 2d and 2e). 2a reacts with KOCl in
