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Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles. / Peshkov, Anatoly A.; Gapanenok, Diana; Puzyk, Aleksandra; Amire, Niyaz; Novikov, Alexander S.; Martynova, Sofia D.; Kalinin, Stanislav; Dar’in, Dmitry; Peshkov, Vsevolod A.; Krasavin, Mikhail.

In: The Journal of organic chemistry, Vol. 88, No. 15, 17.07.2023, p. 10508–10524.

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

Harvard

Peshkov, AA, Gapanenok, D, Puzyk, A, Amire, N, Novikov, AS, Martynova, SD, Kalinin, S, Dar’in, D, Peshkov, VA & Krasavin, M 2023, 'Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles', The Journal of organic chemistry, vol. 88, no. 15, pp. 10508–10524. https://doi.org/10.1021/acs.joc.3c00497

APA

Peshkov, A. A., Gapanenok, D., Puzyk, A., Amire, N., Novikov, A. S., Martynova, S. D., Kalinin, S., Dar’in, D., Peshkov, V. A., & Krasavin, M. (2023). Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles. The Journal of organic chemistry, 88(15), 10508–10524. https://doi.org/10.1021/acs.joc.3c00497

Vancouver

Peshkov AA, Gapanenok D, Puzyk A, Amire N, Novikov AS, Martynova SD et al. Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles. The Journal of organic chemistry. 2023 Jul 17;88(15):10508–10524. https://doi.org/10.1021/acs.joc.3c00497

Author

Peshkov, Anatoly A. ; Gapanenok, Diana ; Puzyk, Aleksandra ; Amire, Niyaz ; Novikov, Alexander S. ; Martynova, Sofia D. ; Kalinin, Stanislav ; Dar’in, Dmitry ; Peshkov, Vsevolod A. ; Krasavin, Mikhail. / Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles. In: The Journal of organic chemistry. 2023 ; Vol. 88, No. 15. pp. 10508–10524.

BibTeX

@article{0bd59556c66f483a831bba62ff0997cd,
title = "Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles",
abstract = "A chemoselective strategy toward a variety of fused heterocyclic scaffolds relying on a three-component condensation of heterocyclic ketene aminals (HKAs) or corresponding thioaminals with aryl glyoxals and cyclic 1,3-dicarbonyl compounds has been developed and explored. Depending on the applied combination of substrates, the strategy can be tuned to provide straightforward access to imidazo[1,2-a]quinoline, pyrrolo[1,2-a]imidazole, and pyrrolo[2,1-b]thiazole frameworks.",
author = "Peshkov, {Anatoly A.} and Diana Gapanenok and Aleksandra Puzyk and Niyaz Amire and Novikov, {Alexander S.} and Martynova, {Sofia D.} and Stanislav Kalinin and Dmitry Dar{\textquoteright}in and Peshkov, {Vsevolod A.} and Mikhail Krasavin",
year = "2023",
month = jul,
day = "17",
doi = "10.1021/acs.joc.3c00497",
language = "English",
volume = "88",
pages = "10508–10524",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "15",

}

RIS

TY - JOUR

T1 - Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles

AU - Peshkov, Anatoly A.

AU - Gapanenok, Diana

AU - Puzyk, Aleksandra

AU - Amire, Niyaz

AU - Novikov, Alexander S.

AU - Martynova, Sofia D.

AU - Kalinin, Stanislav

AU - Dar’in, Dmitry

AU - Peshkov, Vsevolod A.

AU - Krasavin, Mikhail

PY - 2023/7/17

Y1 - 2023/7/17

N2 - A chemoselective strategy toward a variety of fused heterocyclic scaffolds relying on a three-component condensation of heterocyclic ketene aminals (HKAs) or corresponding thioaminals with aryl glyoxals and cyclic 1,3-dicarbonyl compounds has been developed and explored. Depending on the applied combination of substrates, the strategy can be tuned to provide straightforward access to imidazo[1,2-a]quinoline, pyrrolo[1,2-a]imidazole, and pyrrolo[2,1-b]thiazole frameworks.

AB - A chemoselective strategy toward a variety of fused heterocyclic scaffolds relying on a three-component condensation of heterocyclic ketene aminals (HKAs) or corresponding thioaminals with aryl glyoxals and cyclic 1,3-dicarbonyl compounds has been developed and explored. Depending on the applied combination of substrates, the strategy can be tuned to provide straightforward access to imidazo[1,2-a]quinoline, pyrrolo[1,2-a]imidazole, and pyrrolo[2,1-b]thiazole frameworks.

UR - https://www.mendeley.com/catalogue/06ed4aa3-f311-3a54-b6fc-cbca319b219d/

U2 - 10.1021/acs.joc.3c00497

DO - 10.1021/acs.joc.3c00497

M3 - Article

VL - 88

SP - 10508

EP - 10524

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 15

ER -

ID: 107312814