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Multicomponent Assembly of Trisubstituted Imidazoles and Their Photochemical Cyclization into Fused Polyheterocyclic Scaffolds. / Gapanenok, Diana; Makhmet, Azat; Peshkov, Anatoly A.; Smirnova, Darya; Amire, Niyaz; Peshkov, Vsevolod A.; Spiridonova, Darya; Dar'In, Dmitry; Balalaie, Saeed; Krasavin, Mikhail.

в: Journal of Organic Chemistry, Том 87, № 12, 17.06.2022, стр. 7838–7851.

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

Harvard

Gapanenok, D, Makhmet, A, Peshkov, AA, Smirnova, D, Amire, N, Peshkov, VA, Spiridonova, D, Dar'In, D, Balalaie, S & Krasavin, M 2022, 'Multicomponent Assembly of Trisubstituted Imidazoles and Their Photochemical Cyclization into Fused Polyheterocyclic Scaffolds', Journal of Organic Chemistry, Том. 87, № 12, стр. 7838–7851. https://doi.org/10.1021/acs.joc.2c00475

APA

Gapanenok, D., Makhmet, A., Peshkov, A. A., Smirnova, D., Amire, N., Peshkov, V. A., Spiridonova, D., Dar'In, D., Balalaie, S., & Krasavin, M. (2022). Multicomponent Assembly of Trisubstituted Imidazoles and Their Photochemical Cyclization into Fused Polyheterocyclic Scaffolds. Journal of Organic Chemistry, 87(12), 7838–7851. https://doi.org/10.1021/acs.joc.2c00475

Vancouver

Gapanenok D, Makhmet A, Peshkov AA, Smirnova D, Amire N, Peshkov VA и пр. Multicomponent Assembly of Trisubstituted Imidazoles and Their Photochemical Cyclization into Fused Polyheterocyclic Scaffolds. Journal of Organic Chemistry. 2022 Июнь 17;87(12):7838–7851. https://doi.org/10.1021/acs.joc.2c00475

Author

Gapanenok, Diana ; Makhmet, Azat ; Peshkov, Anatoly A. ; Smirnova, Darya ; Amire, Niyaz ; Peshkov, Vsevolod A. ; Spiridonova, Darya ; Dar'In, Dmitry ; Balalaie, Saeed ; Krasavin, Mikhail. / Multicomponent Assembly of Trisubstituted Imidazoles and Their Photochemical Cyclization into Fused Polyheterocyclic Scaffolds. в: Journal of Organic Chemistry. 2022 ; Том 87, № 12. стр. 7838–7851.

BibTeX

@article{4417c758de9d4bcf90cc4744101753e1,
title = "Multicomponent Assembly of Trisubstituted Imidazoles and Their Photochemical Cyclization into Fused Polyheterocyclic Scaffolds",
abstract = "A straightforward route to a large and diverse library of trisubstituted imidazoles was established via a three-component reaction of 2-oxoaldehydes, 1,3-dicarbonyl compounds, and acyclic nitrogen bis-nucleophiles. The obtained products were subsequently explored in a photochemical cyclization yielding a variety of imidazole-fused polycyclic compounds. ",
author = "Diana Gapanenok and Azat Makhmet and Peshkov, {Anatoly A.} and Darya Smirnova and Niyaz Amire and Peshkov, {Vsevolod A.} and Darya Spiridonova and Dmitry Dar'In and Saeed Balalaie and Mikhail Krasavin",
note = "Publisher Copyright: {\textcopyright} 2022 American Chemical Society. All rights reserved.",
year = "2022",
month = jun,
day = "17",
doi = "10.1021/acs.joc.2c00475",
language = "English",
volume = "87",
pages = "7838–7851",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "12",

}

RIS

TY - JOUR

T1 - Multicomponent Assembly of Trisubstituted Imidazoles and Their Photochemical Cyclization into Fused Polyheterocyclic Scaffolds

AU - Gapanenok, Diana

AU - Makhmet, Azat

AU - Peshkov, Anatoly A.

AU - Smirnova, Darya

AU - Amire, Niyaz

AU - Peshkov, Vsevolod A.

AU - Spiridonova, Darya

AU - Dar'In, Dmitry

AU - Balalaie, Saeed

AU - Krasavin, Mikhail

N1 - Publisher Copyright: © 2022 American Chemical Society. All rights reserved.

PY - 2022/6/17

Y1 - 2022/6/17

N2 - A straightforward route to a large and diverse library of trisubstituted imidazoles was established via a three-component reaction of 2-oxoaldehydes, 1,3-dicarbonyl compounds, and acyclic nitrogen bis-nucleophiles. The obtained products were subsequently explored in a photochemical cyclization yielding a variety of imidazole-fused polycyclic compounds.

AB - A straightforward route to a large and diverse library of trisubstituted imidazoles was established via a three-component reaction of 2-oxoaldehydes, 1,3-dicarbonyl compounds, and acyclic nitrogen bis-nucleophiles. The obtained products were subsequently explored in a photochemical cyclization yielding a variety of imidazole-fused polycyclic compounds.

UR - http://www.scopus.com/inward/record.url?scp=85133522409&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/a37c481b-0ae5-3ff3-91b4-71c9a8ac11cd/

U2 - 10.1021/acs.joc.2c00475

DO - 10.1021/acs.joc.2c00475

M3 - Article

AN - SCOPUS:85133522409

VL - 87

SP - 7838

EP - 7851

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 12

ER -

ID: 97239739