Standard

Construction of Annulated Spiro[4.4]-nonane-diones via the Tandem [4 + 2]-Cycloaddition/Aromatization Reaction. / Ivanov, Konstantin S; Samburskiy, Denis E; Zargarova, Leila V et al.

In: Journal of Organic Chemistry, Vol. 88, No. 15, 04.08.2023, p. 11003-11009.

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

Harvard

Ivanov, KS, Samburskiy, DE, Zargarova, LV, Komarov, VY & Mostovich, EA 2023, 'Construction of Annulated Spiro[4.4]-nonane-diones via the Tandem [4 + 2]-Cycloaddition/Aromatization Reaction', Journal of Organic Chemistry, vol. 88, no. 15, pp. 11003-11009. https://doi.org/10.1021/acs.joc.3c00981

APA

Ivanov, K. S., Samburskiy, D. E., Zargarova, L. V., Komarov, V. Y., & Mostovich, E. A. (2023). Construction of Annulated Spiro[4.4]-nonane-diones via the Tandem [4 + 2]-Cycloaddition/Aromatization Reaction. Journal of Organic Chemistry, 88(15), 11003-11009. https://doi.org/10.1021/acs.joc.3c00981

Vancouver

Ivanov KS, Samburskiy DE, Zargarova LV, Komarov VY, Mostovich EA. Construction of Annulated Spiro[4.4]-nonane-diones via the Tandem [4 + 2]-Cycloaddition/Aromatization Reaction. Journal of Organic Chemistry. 2023 Aug 4;88(15):11003-11009. Epub 2023 Jul 18. doi: 10.1021/acs.joc.3c00981

Author

Ivanov, Konstantin S ; Samburskiy, Denis E ; Zargarova, Leila V et al. / Construction of Annulated Spiro[4.4]-nonane-diones via the Tandem [4 + 2]-Cycloaddition/Aromatization Reaction. In: Journal of Organic Chemistry. 2023 ; Vol. 88, No. 15. pp. 11003-11009.

BibTeX

@article{658a2772a30d4c47aff30dab3a13591a,
title = "Construction of Annulated Spiro[4.4]-nonane-diones via the Tandem [4 + 2]-Cycloaddition/Aromatization Reaction",
abstract = "A method for the synthesis of both symmetric and asymmetric fused spiro[4.4]-nonane-dione derivatives has been developed. It is based on a Diels-Alder reaction of spiro[4.4]nona-2,7-diene-1,6-dione as a dienophile component followed by immediate aromatization of the adduct. An active diene component can be generated using the tetrabromoxylene/NaI system, the 1,3-diphenylisobenzofuran/BF3 system, or substituted cyclones.",
author = "Ivanov, {Konstantin S} and Samburskiy, {Denis E} and Zargarova, {Leila V} and Komarov, {Vladislav Yu} and Mostovich, {Evgeny A}",
note = "This work was supported by the Ministry of Science and Higher Education of the Russian Federation under project No. FSUS-2021-0014. Resource Center “VTAN” (Novosibirsk State University) is acknowledged for access to experimental equipment, and Multi-Access Chemical Research Center SB RAS is acknowledged for spectral and analytical measurements.",
year = "2023",
month = aug,
day = "4",
doi = "10.1021/acs.joc.3c00981",
language = "English",
volume = "88",
pages = "11003--11009",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "15",

}

RIS

TY - JOUR

T1 - Construction of Annulated Spiro[4.4]-nonane-diones via the Tandem [4 + 2]-Cycloaddition/Aromatization Reaction

AU - Ivanov, Konstantin S

AU - Samburskiy, Denis E

AU - Zargarova, Leila V

AU - Komarov, Vladislav Yu

AU - Mostovich, Evgeny A

N1 - This work was supported by the Ministry of Science and Higher Education of the Russian Federation under project No. FSUS-2021-0014. Resource Center “VTAN” (Novosibirsk State University) is acknowledged for access to experimental equipment, and Multi-Access Chemical Research Center SB RAS is acknowledged for spectral and analytical measurements.

PY - 2023/8/4

Y1 - 2023/8/4

N2 - A method for the synthesis of both symmetric and asymmetric fused spiro[4.4]-nonane-dione derivatives has been developed. It is based on a Diels-Alder reaction of spiro[4.4]nona-2,7-diene-1,6-dione as a dienophile component followed by immediate aromatization of the adduct. An active diene component can be generated using the tetrabromoxylene/NaI system, the 1,3-diphenylisobenzofuran/BF3 system, or substituted cyclones.

AB - A method for the synthesis of both symmetric and asymmetric fused spiro[4.4]-nonane-dione derivatives has been developed. It is based on a Diels-Alder reaction of spiro[4.4]nona-2,7-diene-1,6-dione as a dienophile component followed by immediate aromatization of the adduct. An active diene component can be generated using the tetrabromoxylene/NaI system, the 1,3-diphenylisobenzofuran/BF3 system, or substituted cyclones.

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85166432133&origin=inward&txGid=5511259439491786069bbc0f3ddd8ab1

UR - https://www.mendeley.com/catalogue/07ff1c0d-b8ea-32e2-8bca-6a7ce54f6cdf/

U2 - 10.1021/acs.joc.3c00981

DO - 10.1021/acs.joc.3c00981

M3 - Article

C2 - 37462945

VL - 88

SP - 11003

EP - 11009

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 15

ER -

ID: 52708401