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Heteroannelated Enaminoketones Derived from 1,2,4-Triketone Analogs. / Edilova, Yu.; Kudyakova, Yu.; Slepukhin, P. et al.
In: Russian Journal of General Chemistry, Vol. 93, No. S1, 2023, p. S10-S18.

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

Harvard

Edilova, Y, Kudyakova, Y, Slepukhin, P, Saloutin, V & Bazhin, D 2023, 'Heteroannelated Enaminoketones Derived from 1,2,4-Triketone Analogs', Russian Journal of General Chemistry, vol. 93, no. S1, pp. S10-S18. https://doi.org/10.1134/S1070363223140098

APA

Edilova, Y., Kudyakova, Y., Slepukhin, P., Saloutin, V., & Bazhin, D. (2023). Heteroannelated Enaminoketones Derived from 1,2,4-Triketone Analogs. Russian Journal of General Chemistry, 93(S1), S10-S18. https://doi.org/10.1134/S1070363223140098

Vancouver

Edilova Y, Kudyakova Y, Slepukhin P, Saloutin V, Bazhin D. Heteroannelated Enaminoketones Derived from 1,2,4-Triketone Analogs. Russian Journal of General Chemistry. 2023;93(S1):S10-S18. doi: 10.1134/S1070363223140098

Author

Edilova, Yu. ; Kudyakova, Yu. ; Slepukhin, P. et al. / Heteroannelated Enaminoketones Derived from 1,2,4-Triketone Analogs. In: Russian Journal of General Chemistry. 2023 ; Vol. 93, No. S1. pp. S10-S18.

BibTeX

@article{98643944cc694e478fae7c2506ce7b26,
title = "Heteroannelated Enaminoketones Derived from 1,2,4-Triketone Analogs",
abstract = "The reaction of (perfluoroalkyl)furan-3(2H)-ones and β-diketone containing an acetal moiety with (hetero)aromatic 1,2-diamines was studied. Quinoxalines and pyrido[3,4-b]pyrazine bearing the enaminoketone fragment were ynthesized by the regioselective addition of a dinucleophile at the α-dicarbonyl moiety of polyketones. In the case of β-diketone containing acetal and ester groups, the conversion involves the α-ketoester moiety to form a quinoxalinyl-substituted 2,3-butanedione. All products were characterized by NMR spectroscopy and X-ray diffraction. {\textcopyright} 2023, Pleiades Publishing, Ltd.",
author = "Yu. Edilova and Yu. Kudyakova and P. Slepukhin and V. Saloutin and D. Bazhin",
note = "The work was financially supported by the Russian Science Foundation (project no. 23-23-00425, https://rscf.ru/en/project/23-23-00425/) ).",
year = "2023",
doi = "10.1134/S1070363223140098",
language = "English",
volume = "93",
pages = "S10--S18",
journal = "Russian Journal of General Chemistry",
issn = "1070-3632",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "S1",

}

RIS

TY - JOUR

T1 - Heteroannelated Enaminoketones Derived from 1,2,4-Triketone Analogs

AU - Edilova, Yu.

AU - Kudyakova, Yu.

AU - Slepukhin, P.

AU - Saloutin, V.

AU - Bazhin, D.

N1 - The work was financially supported by the Russian Science Foundation (project no. 23-23-00425, https://rscf.ru/en/project/23-23-00425/) ).

PY - 2023

Y1 - 2023

N2 - The reaction of (perfluoroalkyl)furan-3(2H)-ones and β-diketone containing an acetal moiety with (hetero)aromatic 1,2-diamines was studied. Quinoxalines and pyrido[3,4-b]pyrazine bearing the enaminoketone fragment were ynthesized by the regioselective addition of a dinucleophile at the α-dicarbonyl moiety of polyketones. In the case of β-diketone containing acetal and ester groups, the conversion involves the α-ketoester moiety to form a quinoxalinyl-substituted 2,3-butanedione. All products were characterized by NMR spectroscopy and X-ray diffraction. © 2023, Pleiades Publishing, Ltd.

AB - The reaction of (perfluoroalkyl)furan-3(2H)-ones and β-diketone containing an acetal moiety with (hetero)aromatic 1,2-diamines was studied. Quinoxalines and pyrido[3,4-b]pyrazine bearing the enaminoketone fragment were ynthesized by the regioselective addition of a dinucleophile at the α-dicarbonyl moiety of polyketones. In the case of β-diketone containing acetal and ester groups, the conversion involves the α-ketoester moiety to form a quinoxalinyl-substituted 2,3-butanedione. All products were characterized by NMR spectroscopy and X-ray diffraction. © 2023, Pleiades Publishing, Ltd.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85178962957

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=001117621900034

U2 - 10.1134/S1070363223140098

DO - 10.1134/S1070363223140098

M3 - Article

VL - 93

SP - S10-S18

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - S1

ER -

ID: 49825187