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2 H-Azirines as C-C Annulation Reagents in Cu-Catalyzed Synthesis of Furo[3,2-c]quinolone Derivatives. / Sakharov, Pavel A.; Rostovskii, Nikolai V.; Khlebnikov, Alexander F.; Panikorovskii, Taras L.; Novikov, Mikhail S.

в: Organic Letters, Том 21, № 10, 17.05.2019, стр. 3615-3619.

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

Harvard

Sakharov, PA, Rostovskii, NV, Khlebnikov, AF, Panikorovskii, TL & Novikov, MS 2019, '2 H-Azirines as C-C Annulation Reagents in Cu-Catalyzed Synthesis of Furo[3,2-c]quinolone Derivatives', Organic Letters, Том. 21, № 10, стр. 3615-3619. https://doi.org/10.1021/acs.orglett.9b01043

APA

Sakharov, P. A., Rostovskii, N. V., Khlebnikov, A. F., Panikorovskii, T. L., & Novikov, M. S. (2019). 2 H-Azirines as C-C Annulation Reagents in Cu-Catalyzed Synthesis of Furo[3,2-c]quinolone Derivatives. Organic Letters, 21(10), 3615-3619. https://doi.org/10.1021/acs.orglett.9b01043

Vancouver

Sakharov PA, Rostovskii NV, Khlebnikov AF, Panikorovskii TL, Novikov MS. 2 H-Azirines as C-C Annulation Reagents in Cu-Catalyzed Synthesis of Furo[3,2-c]quinolone Derivatives. Organic Letters. 2019 Май 17;21(10):3615-3619. https://doi.org/10.1021/acs.orglett.9b01043

Author

Sakharov, Pavel A. ; Rostovskii, Nikolai V. ; Khlebnikov, Alexander F. ; Panikorovskii, Taras L. ; Novikov, Mikhail S. / 2 H-Azirines as C-C Annulation Reagents in Cu-Catalyzed Synthesis of Furo[3,2-c]quinolone Derivatives. в: Organic Letters. 2019 ; Том 21, № 10. стр. 3615-3619.

BibTeX

@article{28ee9c06e4c246d29d2e43d7e800e2a4,
title = "2 H-Azirines as C-C Annulation Reagents in Cu-Catalyzed Synthesis of Furo[3,2-c]quinolone Derivatives",
abstract = "A method of furo-annulation of 4-hydroxy-2-oxoquinoline-3-carboxylates with 3-arylazirines under Cu(II) catalysis was developed to synthesize a variety of 2,3-dihydrofuro[3,2-c]quinolones bearing a carbamate group at the C2 position. The reaction involves an azirine ring opening across the N-C2 bond and formation of a dihydrofuran ring with the inclusion of two azirine carbon atoms, accompanied by a shift of the ester group to the nitrogen. The discovered reaction is the first example of the use of 2H-azirines for furo-annulation.",
author = "Sakharov, {Pavel A.} and Rostovskii, {Nikolai V.} and Khlebnikov, {Alexander F.} and Panikorovskii, {Taras L.} and Novikov, {Mikhail S.}",
year = "2019",
month = may,
day = "17",
doi = "10.1021/acs.orglett.9b01043",
language = "English",
volume = "21",
pages = "3615--3619",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "10",

}

RIS

TY - JOUR

T1 - 2 H-Azirines as C-C Annulation Reagents in Cu-Catalyzed Synthesis of Furo[3,2-c]quinolone Derivatives

AU - Sakharov, Pavel A.

AU - Rostovskii, Nikolai V.

AU - Khlebnikov, Alexander F.

AU - Panikorovskii, Taras L.

AU - Novikov, Mikhail S.

PY - 2019/5/17

Y1 - 2019/5/17

N2 - A method of furo-annulation of 4-hydroxy-2-oxoquinoline-3-carboxylates with 3-arylazirines under Cu(II) catalysis was developed to synthesize a variety of 2,3-dihydrofuro[3,2-c]quinolones bearing a carbamate group at the C2 position. The reaction involves an azirine ring opening across the N-C2 bond and formation of a dihydrofuran ring with the inclusion of two azirine carbon atoms, accompanied by a shift of the ester group to the nitrogen. The discovered reaction is the first example of the use of 2H-azirines for furo-annulation.

AB - A method of furo-annulation of 4-hydroxy-2-oxoquinoline-3-carboxylates with 3-arylazirines under Cu(II) catalysis was developed to synthesize a variety of 2,3-dihydrofuro[3,2-c]quinolones bearing a carbamate group at the C2 position. The reaction involves an azirine ring opening across the N-C2 bond and formation of a dihydrofuran ring with the inclusion of two azirine carbon atoms, accompanied by a shift of the ester group to the nitrogen. The discovered reaction is the first example of the use of 2H-azirines for furo-annulation.

UR - http://www.scopus.com/inward/record.url?scp=85065847330&partnerID=8YFLogxK

U2 - 10.1021/acs.orglett.9b01043

DO - 10.1021/acs.orglett.9b01043

M3 - Article

C2 - 31063384

AN - SCOPUS:85065847330

VL - 21

SP - 3615

EP - 3619

JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 10

ER -

ID: 42845410