Abstract:
Reactions of 3-arylpropynoic acid derivatives and conjugated acetylene ketones with arenes and cyclohexane under the action of AlCl3 at room temperature for 15 h afford the corresponding products of one-pot tandem hydroarylation–ionic hydrogenation of the acetylene bond of the starting compounds in 42–98% yields. This reaction is accompanied by aryl group exchange process under acidic conditions.
Citation:
I. I. Ignatova, O. V. Khoroshilova, A. V. Vasilyev, “Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one”, Mendeleev Commun., 33:1 (2023), 27–29
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https://www.mathnet.ru/eng/mendc297
https://www.mathnet.ru/eng/mendc/v33/i1/p27
This publication is cited in the following 2 articles:
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