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Sebelius, S., Olsson, V.J., Wallner, O.A. and Szabo, K.J. (2006) Palladium-Catalyzed Coupling of Allylboronic Acids with Iodobenzenes. Selective Formation of the Branched Allylic Product in the Absence of Directing Groups. Journal of the American Chemical Society, 128, 8150-8151.
https://doi.org/10.1021/ja062585o

has been cited by the following article:

• TITLE: Pd-Catalyzed Microwave Irradiated Regioselective Aroylation Reaction of Crotyl- and Allyltrifluoroborates

  AUTHORS: Mohammad Al-Masum, Sarah Legan, Kwei-Yu Liu

  KEYWORDS: Direct Aroylation, Regioselectivity, Stereoselectivity, Microwave

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.6 No.4, December 20, 2016

  ABSTRACT: An interesting regioselectivity is observed when the mixture of potassium crotyltrifluoroborate (1a) and aroyl chlorides having electron-deficient and electron-rich groups is microwaved in the presence of palladium-catalyst. In the case of electron withdrawing group with phenyl ring of aroyl chlorides, isomerized α,β-unsaturated compound 3 is the product whereas electron donating group with phenyl ring of aroyl chlorides furnishes α-adduct 4. Similar aroylation reaction is also established for potassium allyltrifluoroborate (1b). In this case, regioselectivity is unaffected with changing electron-rich or electron-deficient groups in phenyl ring of the aroyl chlorides. Reactions proceed with, essentially in same rate, affording the corresponding aryl propenyl ketones (crotonophenones) 5 in good to high yields.