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The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones. / Viktorova, Viktoria V.; Steparuk, Elena V.; Obydennov, Dmitrii L. et al.
In: Molecules, Vol. 28, No. 3, 1285, 01.2023.

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

Harvard

Viktorova, VV, Steparuk, EV, Obydennov, DL & Sosnovskikh, VY 2023, 'The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones', Molecules, vol. 28, no. 3, 1285. https://doi.org/10.3390/molecules28031285

APA

Viktorova, V. V., Steparuk, E. V., Obydennov, D. L., & Sosnovskikh, V. Y. (2023). The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones. Molecules, 28(3), [1285]. https://doi.org/10.3390/molecules28031285

Vancouver

Viktorova VV, Steparuk EV, Obydennov DL, Sosnovskikh VY. The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones. Molecules. 2023 Jan;28(3):1285. doi: 10.3390/molecules28031285

Author

Viktorova, Viktoria V. ; Steparuk, Elena V. ; Obydennov, Dmitrii L. et al. / The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones. In: Molecules. 2023 ; Vol. 28, No. 3.

BibTeX

@article{810e860b880642f2aa77332e766e81a6,
title = "The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones",
abstract = "This work describes the synthesis of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones, their tautomerism, and reactivity towards binucleophiles. These molecules are novel and convenient building-blocks for the direct construction of biologically important polycyclic pyridones via an oxazinone ring-opening transformation promoted with ammonium acetate or acetic acid. In the case of o-phenylenediamine, partial aromatization of the obtained heterocycles proceeded to form polycyclic benzimidazole-fused pyridones (33-91%).",
author = "Viktorova, {Viktoria V.} and Steparuk, {Elena V.} and Obydennov, {Dmitrii L.} and Sosnovskikh, {Vyacheslav Y.}",
note = "The research funding from the Ministry of Science and Higher Education of the Russian Federation (Ural Federal University Program of Development within the Priority-2030 Program) is gratefully acknowledged.",
year = "2023",
month = jan,
doi = "10.3390/molecules28031285",
language = "English",
volume = "28",
journal = "Molecules",
issn = "1420-3049",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "3",

}

RIS

TY - JOUR

T1 - The Construction of Polycyclic Pyridones via Ring-Opening Transformations of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones

AU - Viktorova, Viktoria V.

AU - Steparuk, Elena V.

AU - Obydennov, Dmitrii L.

AU - Sosnovskikh, Vyacheslav Y.

N1 - The research funding from the Ministry of Science and Higher Education of the Russian Federation (Ural Federal University Program of Development within the Priority-2030 Program) is gratefully acknowledged.

PY - 2023/1

Y1 - 2023/1

N2 - This work describes the synthesis of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones, their tautomerism, and reactivity towards binucleophiles. These molecules are novel and convenient building-blocks for the direct construction of biologically important polycyclic pyridones via an oxazinone ring-opening transformation promoted with ammonium acetate or acetic acid. In the case of o-phenylenediamine, partial aromatization of the obtained heterocycles proceeded to form polycyclic benzimidazole-fused pyridones (33-91%).

AB - This work describes the synthesis of 3-hydroxy-3,4-dihydropyrido[2,1-c][1,4]oxazine-1,8-diones, their tautomerism, and reactivity towards binucleophiles. These molecules are novel and convenient building-blocks for the direct construction of biologically important polycyclic pyridones via an oxazinone ring-opening transformation promoted with ammonium acetate or acetic acid. In the case of o-phenylenediamine, partial aromatization of the obtained heterocycles proceeded to form polycyclic benzimidazole-fused pyridones (33-91%).

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85147893723

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000933749700001

U2 - 10.3390/molecules28031285

DO - 10.3390/molecules28031285

M3 - Article

VL - 28

JO - Molecules

JF - Molecules

SN - 1420-3049

IS - 3

M1 - 1285

ER -

ID: 34719285