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Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3·Et2O–H2O Catalytic System. / Il’ina, Irina V.; Patrusheva, Oksana S.; Korchagina, Dina V. et al.

In: Chemistry of Heterocyclic Compounds, Vol. 56, No. 7, 01.07.2020, p. 867-874.

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

Harvard

Il’ina, IV, Patrusheva, OS, Korchagina, DV, Volcho, KP & Salakhutdinov, NF 2020, 'Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3·Et2O–H2O Catalytic System', Chemistry of Heterocyclic Compounds, vol. 56, no. 7, pp. 867-874. https://doi.org/10.1007/s10593-020-02743-z

APA

Il’ina, I. V., Patrusheva, O. S., Korchagina, D. V., Volcho, K. P., & Salakhutdinov, N. F. (2020). Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3·Et2O–H2O Catalytic System. Chemistry of Heterocyclic Compounds, 56(7), 867-874. https://doi.org/10.1007/s10593-020-02743-z

Vancouver

Il’ina IV, Patrusheva OS, Korchagina DV, Volcho KP, Salakhutdinov NF. Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3·Et2O–H2O Catalytic System. Chemistry of Heterocyclic Compounds. 2020 Jul 1;56(7):867-874. doi: 10.1007/s10593-020-02743-z

Author

Il’ina, Irina V. ; Patrusheva, Oksana S. ; Korchagina, Dina V. et al. / Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3·Et2O–H2O Catalytic System. In: Chemistry of Heterocyclic Compounds. 2020 ; Vol. 56, No. 7. pp. 867-874.

BibTeX

@article{217004192e20465a839b72705ffdd91b,
title = "Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3·Et2O–H2O Catalytic System",
abstract = "The synthesis of fluorinated octahydro-2H-chromene was carried out using the Prins reaction between the monoterpenoid (–)-isopulegol and carbonyl compounds in the presence of the BF3·Et2O–H2O system, which acts as both an acid catalyst and a fluorine source. The use of the readily available and easy-to-use BF3·Et2O reagent makes this method of obtaining fluorine derivatives simple and practical.",
keywords = "acid catalysts, boron trifluoride etherate, chromene, isopulegol, monoterpenes, organofluorine compounds, Prins reaction, REAGENT, ACID, TETRAHYDROPYRANS, ISOPULEGOL, DISCOVERY, PRINS CYCLIZATION, VANILLIN, POTENT ANALGESIC ACTIVITY",
author = "Il{\textquoteright}ina, {Irina V.} and Patrusheva, {Oksana S.} and Korchagina, {Dina V.} and Volcho, {Konstantin P.} and Salakhutdinov, {Nariman F.}",
year = "2020",
month = jul,
day = "1",
doi = "10.1007/s10593-020-02743-z",
language = "English",
volume = "56",
pages = "867--874",
journal = "Chemistry of Heterocyclic Compounds",
issn = "0009-3122",
publisher = "Springer New York",
number = "7",

}

RIS

TY - JOUR

T1 - Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3·Et2O–H2O Catalytic System

AU - Il’ina, Irina V.

AU - Patrusheva, Oksana S.

AU - Korchagina, Dina V.

AU - Volcho, Konstantin P.

AU - Salakhutdinov, Nariman F.

PY - 2020/7/1

Y1 - 2020/7/1

N2 - The synthesis of fluorinated octahydro-2H-chromene was carried out using the Prins reaction between the monoterpenoid (–)-isopulegol and carbonyl compounds in the presence of the BF3·Et2O–H2O system, which acts as both an acid catalyst and a fluorine source. The use of the readily available and easy-to-use BF3·Et2O reagent makes this method of obtaining fluorine derivatives simple and practical.

AB - The synthesis of fluorinated octahydro-2H-chromene was carried out using the Prins reaction between the monoterpenoid (–)-isopulegol and carbonyl compounds in the presence of the BF3·Et2O–H2O system, which acts as both an acid catalyst and a fluorine source. The use of the readily available and easy-to-use BF3·Et2O reagent makes this method of obtaining fluorine derivatives simple and practical.

KW - acid catalysts

KW - boron trifluoride etherate

KW - chromene

KW - isopulegol

KW - monoterpenes

KW - organofluorine compounds

KW - Prins reaction

KW - REAGENT

KW - ACID

KW - TETRAHYDROPYRANS

KW - ISOPULEGOL

KW - DISCOVERY

KW - PRINS CYCLIZATION

KW - VANILLIN

KW - POTENT ANALGESIC ACTIVITY

UR - http://www.scopus.com/inward/record.url?scp=85089725054&partnerID=8YFLogxK

U2 - 10.1007/s10593-020-02743-z

DO - 10.1007/s10593-020-02743-z

M3 - Article

AN - SCOPUS:85089725054

VL - 56

SP - 867

EP - 874

JO - Chemistry of Heterocyclic Compounds

JF - Chemistry of Heterocyclic Compounds

SN - 0009-3122

IS - 7

ER -

ID: 25093949