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Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond. / Smorodina, Anastasia; Buev, Evgeny; Moshkin, Vladimir et al.
In: Tetrahedron Letters, Vol. 133, 154830, 01.12.2023.

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

Harvard

Smorodina, A, Buev, E, Moshkin, V & Sosnovskikh, V 2023, 'Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond', Tetrahedron Letters, vol. 133, 154830. https://doi.org/10.1016/j.tetlet.2023.154830

APA

Smorodina, A., Buev, E., Moshkin, V., & Sosnovskikh, V. (2023). Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond. Tetrahedron Letters, 133, [154830]. https://doi.org/10.1016/j.tetlet.2023.154830

Vancouver

Smorodina A, Buev E, Moshkin V, Sosnovskikh V. Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond. Tetrahedron Letters. 2023 Dec 1;133:154830. doi: 10.1016/j.tetlet.2023.154830

Author

Smorodina, Anastasia ; Buev, Evgeny ; Moshkin, Vladimir et al. / Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond. In: Tetrahedron Letters. 2023 ; Vol. 133.

BibTeX

@article{fb525312d67144ca85804e51a206f882,
title = "Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond",
abstract = "Reaction of 3,3-diacylpyrrolidines with hydrazines in ethanol leads to the formation of 2-pyrazolylethylamines in 41–100% yields.",
author = "Anastasia Smorodina and Evgeny Buev and Vladimir Moshkin and Vyacheslav Sosnovskikh",
note = "This work was financially supported by the Russian Science Foundation (Grant 23-23-00201).",
year = "2023",
month = dec,
day = "1",
doi = "10.1016/j.tetlet.2023.154830",
language = "English",
volume = "133",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Recyclization of 3,3-diacylpyrrolidines into pyrazolylethylamines: Pyrazole aromaticity vs pyrrolidine C - C bond

AU - Smorodina, Anastasia

AU - Buev, Evgeny

AU - Moshkin, Vladimir

AU - Sosnovskikh, Vyacheslav

N1 - This work was financially supported by the Russian Science Foundation (Grant 23-23-00201).

PY - 2023/12/1

Y1 - 2023/12/1

N2 - Reaction of 3,3-diacylpyrrolidines with hydrazines in ethanol leads to the formation of 2-pyrazolylethylamines in 41–100% yields.

AB - Reaction of 3,3-diacylpyrrolidines with hydrazines in ethanol leads to the formation of 2-pyrazolylethylamines in 41–100% yields.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85177185921

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=001121881400001

U2 - 10.1016/j.tetlet.2023.154830

DO - 10.1016/j.tetlet.2023.154830

M3 - Article

VL - 133

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

M1 - 154830

ER -

ID: 48494211