Standard

1H,1H,7H-Dodecafluoroheptyl Pentafluorobenzoate. / Kascheeva, Sofia S.; Lastovka, Anastasiya V.; Vinogradov, Andrey S. и др.

в: MolBank, Том 2025, № 3, M2053, 27.08.2025.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Kascheeva, SS, Lastovka, AV, Vinogradov, AS & Parkhomenko, DA 2025, '1H,1H,7H-Dodecafluoroheptyl Pentafluorobenzoate', MolBank, Том. 2025, № 3, M2053. https://doi.org/10.3390/M2053

APA

Kascheeva, S. S., Lastovka, A. V., Vinogradov, A. S., & Parkhomenko, D. A. (2025). 1H,1H,7H-Dodecafluoroheptyl Pentafluorobenzoate. MolBank, 2025(3), [M2053]. https://doi.org/10.3390/M2053

Vancouver

Kascheeva SS, Lastovka AV, Vinogradov AS, Parkhomenko DA. 1H,1H,7H-Dodecafluoroheptyl Pentafluorobenzoate. MolBank. 2025 авг. 27;2025(3):M2053. doi: 10.3390/M2053

Author

Kascheeva, Sofia S. ; Lastovka, Anastasiya V. ; Vinogradov, Andrey S. и др. / 1H,1H,7H-Dodecafluoroheptyl Pentafluorobenzoate. в: MolBank. 2025 ; Том 2025, № 3.

BibTeX

@article{69508beae0a04a089179e1c5f06862f0,
title = "1H,1H,7H-Dodecafluoroheptyl Pentafluorobenzoate",
abstract = "Polyfluoroarenes are widely used in organic synthesis because they readily undergo nucleophilic substitution reactions. This reactivity prompted us to report the synthesis and spectroscopic characterization of a new compound, 1H,1H,7H-dodecafluoroheptyl pentafluorobenzoate, obtained via three different approaches starting from pentafluorobenzoic acid and 1H,1H,7H-dodecafluoroheptanol.",
keywords = "Steglich-type esterification, acid-catalyzed esterification, acyl chloride alcoholysis, ester, polyfluoroarenes",
author = "Kascheeva, {Sofia S.} and Lastovka, {Anastasiya V.} and Vinogradov, {Andrey S.} and Parkhomenko, {Dmitriy A.}",
note = "This research was funded by Russian Science Foundation, grant number 25-23-00445, https://rscf.ru/project/25-23-00445/. 1H,1H,7H-Dodecafluoroheptyl Pentafluorobenzoate / S. S. Kascheeva, A. V. Lastovka, A. S. Vinogradov, D. A. Parkhomenko // MolBank. - Т. 2025. № 3. - С. M2053",
year = "2025",
month = aug,
day = "27",
doi = "10.3390/M2053",
language = "English",
volume = "2025",
journal = "MolBank",
issn = "1422-8599",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "3",

}

RIS

TY - JOUR

T1 - 1H,1H,7H-Dodecafluoroheptyl Pentafluorobenzoate

AU - Kascheeva, Sofia S.

AU - Lastovka, Anastasiya V.

AU - Vinogradov, Andrey S.

AU - Parkhomenko, Dmitriy A.

N1 - This research was funded by Russian Science Foundation, grant number 25-23-00445, https://rscf.ru/project/25-23-00445/. 1H,1H,7H-Dodecafluoroheptyl Pentafluorobenzoate / S. S. Kascheeva, A. V. Lastovka, A. S. Vinogradov, D. A. Parkhomenko // MolBank. - Т. 2025. № 3. - С. M2053

PY - 2025/8/27

Y1 - 2025/8/27

N2 - Polyfluoroarenes are widely used in organic synthesis because they readily undergo nucleophilic substitution reactions. This reactivity prompted us to report the synthesis and spectroscopic characterization of a new compound, 1H,1H,7H-dodecafluoroheptyl pentafluorobenzoate, obtained via three different approaches starting from pentafluorobenzoic acid and 1H,1H,7H-dodecafluoroheptanol.

AB - Polyfluoroarenes are widely used in organic synthesis because they readily undergo nucleophilic substitution reactions. This reactivity prompted us to report the synthesis and spectroscopic characterization of a new compound, 1H,1H,7H-dodecafluoroheptyl pentafluorobenzoate, obtained via three different approaches starting from pentafluorobenzoic acid and 1H,1H,7H-dodecafluoroheptanol.

KW - Steglich-type esterification

KW - acid-catalyzed esterification

KW - acyl chloride alcoholysis

KW - ester

KW - polyfluoroarenes

UR - https://www.mendeley.com/catalogue/9bcca750-6b3f-3d51-a9a8-f256e4989c14/

UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105017846190&origin=inward

U2 - 10.3390/M2053

DO - 10.3390/M2053

M3 - Article

VL - 2025

JO - MolBank

JF - MolBank

SN - 1422-8599

IS - 3

M1 - M2053

ER -

ID: 70629497