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Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid. / Zalivatskaya, Anna S.; Golovanov, Aleksander; Vasilyev, Aleksander V.

In: Chemistry of Heterocyclic Compounds, Vol. 56, No. 7, 01.07.2020, p. 953-956.

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

Harvard

Zalivatskaya, AS, Golovanov, A & Vasilyev, AV 2020, 'Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid', Chemistry of Heterocyclic Compounds, vol. 56, no. 7, pp. 953-956. https://doi.org/10.1007/s10593-020-02756-8

APA

Zalivatskaya, A. S., Golovanov, A., & Vasilyev, A. V. (2020). Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid. Chemistry of Heterocyclic Compounds, 56(7), 953-956. https://doi.org/10.1007/s10593-020-02756-8

Vancouver

Zalivatskaya AS, Golovanov A, Vasilyev AV. Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid. Chemistry of Heterocyclic Compounds. 2020 Jul 1;56(7):953-956. https://doi.org/10.1007/s10593-020-02756-8

Author

Zalivatskaya, Anna S. ; Golovanov, Aleksander ; Vasilyev, Aleksander V. / Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid. In: Chemistry of Heterocyclic Compounds. 2020 ; Vol. 56, No. 7. pp. 953-956.

BibTeX

@article{1e29cd67ab40435bbe1f898659db5176,
title = "Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid",
abstract = "Under the action of an excess of trifluoromethanesulfonic acid, 1-aryl-5-phenylpent-4-en-2-yn-1-ones cyclize intramolecularly to 6-aryl-2-phenyl-2,3-dihydropyran-4-ones. The reaction proceeds at room temperature for 1 h with 50-60% yields.",
keywords = "carbocations, conjugated enynones, cyclization, dihydropyranones, trifluoromethanesulfonic acid, CONJUGATED ENYNONES",
author = "Zalivatskaya, {Anna S.} and Aleksander Golovanov and Vasilyev, {Aleksander V.}",
note = "Funding Information: This work was supported by the Russian Foundation for Basic Research (grant 18-13-00008). Publisher Copyright: {\textcopyright} 2020, Springer Science+Business Media, LLC, part of Springer Nature. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.",
year = "2020",
month = jul,
day = "1",
doi = "10.1007/s10593-020-02756-8",
language = "English",
volume = "56",
pages = "953--956",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer Nature",
number = "7",

}

RIS

TY - JOUR

T1 - Cyclization of 1-Aryl-5-Phenylpent-4-en-2-yn-1-Ones to 2,3-Dihydropyran-2-Ones in Trifluoromethanesulfonic Acid

AU - Zalivatskaya, Anna S.

AU - Golovanov, Aleksander

AU - Vasilyev, Aleksander V.

N1 - Funding Information: This work was supported by the Russian Foundation for Basic Research (grant 18-13-00008). Publisher Copyright: © 2020, Springer Science+Business Media, LLC, part of Springer Nature. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.

PY - 2020/7/1

Y1 - 2020/7/1

N2 - Under the action of an excess of trifluoromethanesulfonic acid, 1-aryl-5-phenylpent-4-en-2-yn-1-ones cyclize intramolecularly to 6-aryl-2-phenyl-2,3-dihydropyran-4-ones. The reaction proceeds at room temperature for 1 h with 50-60% yields.

AB - Under the action of an excess of trifluoromethanesulfonic acid, 1-aryl-5-phenylpent-4-en-2-yn-1-ones cyclize intramolecularly to 6-aryl-2-phenyl-2,3-dihydropyran-4-ones. The reaction proceeds at room temperature for 1 h with 50-60% yields.

KW - carbocations

KW - conjugated enynones

KW - cyclization

KW - dihydropyranones

KW - trifluoromethanesulfonic acid

KW - CONJUGATED ENYNONES

UR - http://www.scopus.com/inward/record.url?scp=85089727263&partnerID=8YFLogxK

U2 - 10.1007/s10593-020-02756-8

DO - 10.1007/s10593-020-02756-8

M3 - Article

AN - SCOPUS:85089727263

VL - 56

SP - 953

EP - 956

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 7

ER -

ID: 69889836