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Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one. / Ignatova, Irina I.; Khoroshilova, Olesya V.; Vasilyev, Aleksander V.

In: Mendeleev Communications, Vol. 33, No. 1, 12.01.2023, p. 27-29.

Research output: Contribution to journal › Article › peer-review

Harvard

Ignatova, II, Khoroshilova, OV & Vasilyev, AV 2023, 'Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one', Mendeleev Communications, vol. 33, no. 1, pp. 27-29. https://doi.org/10.1016/j.mencom.2023.01.008, https://doi.org/10.1016/j.mencom.2023.01.008

APA

Ignatova, I. I., Khoroshilova, O. V., & Vasilyev, A. V. (2023). Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one. Mendeleev Communications, 33(1), 27-29. https://doi.org/10.1016/j.mencom.2023.01.008, https://doi.org/10.1016/j.mencom.2023.01.008

Vancouver

Ignatova II, Khoroshilova OV, Vasilyev AV. Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one. Mendeleev Communications. 2023 Jan 12;33(1):27-29. https://doi.org/10.1016/j.mencom.2023.01.008, https://doi.org/10.1016/j.mencom.2023.01.008

Author

Ignatova, Irina I. ; Khoroshilova, Olesya V. ; Vasilyev, Aleksander V. / Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one. In: Mendeleev Communications. 2023 ; Vol. 33, No. 1. pp. 27-29.

BibTeX

@article{de4dc450990d4a8a8bc7a0ef20e1ace0,
title = "Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one",
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.",
keywords = "arylpropynoic acids, carbocations, hydroarylation, ionic hydrogenation, superelectrophilic activation, ynones",
author = "Ignatova, {Irina I.} and Khoroshilova, {Olesya V.} and Vasilyev, {Aleksander V.}",
note = "Ignatova I.I., Khoroshilova O.V., Vasilyev A.V. Aliminium trichloride-promoted tandem hydroarylation-ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one. Mendeleev Communications. 2023, V. 33, N. 1, P. 27-29.",
year = "2023",
month = jan,
day = "12",
doi = "10.1016/j.mencom.2023.01.008",
language = "English",
volume = "33",
pages = "27--29",
journal = "Mendeleev Communications",
issn = "0959-9436",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Aluminium trichloride-promoted tandem hydroarylation–ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one

AU - Ignatova, Irina I.

AU - Khoroshilova, Olesya V.

AU - Vasilyev, Aleksander V.

N1 - Ignatova I.I., Khoroshilova O.V., Vasilyev A.V. Aliminium trichloride-promoted tandem hydroarylation-ionic hydrogenation of 3-arylpropynoic acid derivatives and 4-phenylbut-3-yn-2-one. Mendeleev Communications. 2023, V. 33, N. 1, P. 27-29.

PY - 2023/1/12

Y1 - 2023/1/12

N2 - 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.

AB - 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.

KW - arylpropynoic acids

KW - carbocations

KW - hydroarylation

KW - ionic hydrogenation

KW - superelectrophilic activation

KW - ynones

UR - https://www.mendeley.com/catalogue/3a155219-9343-3255-93ce-b92f78868700/

U2 - 10.1016/j.mencom.2023.01.008

DO - 10.1016/j.mencom.2023.01.008

M3 - Article

VL - 33

SP - 27

EP - 29

JO - Mendeleev Communications

JF - Mendeleev Communications

SN - 0959-9436

IS - 1

ER -

ID: 113728663