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Regio- and diastereoselectivity of the cycloaddition of nitrones with N-propadienylindole and pyrroles. / Efremova, M.M.; Novikov, A.S.; Kostikov, R.R.; Panikorovsky, T.L.; Ivanov, A.V.; Molchanov, A.P.

в: Tetrahedron, Том 74, № 1, 04.01.2018, стр. 174-183.

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

Harvard

Efremova, MM, Novikov, AS, Kostikov, RR, Panikorovsky, TL, Ivanov, AV & Molchanov, AP 2018, 'Regio- and diastereoselectivity of the cycloaddition of nitrones with N-propadienylindole and pyrroles', Tetrahedron, Том. 74, № 1, стр. 174-183. https://doi.org/10.1016/j.tet.2017.11.056

APA

Efremova, M. M., Novikov, A. S., Kostikov, R. R., Panikorovsky, T. L., Ivanov, A. V., & Molchanov, A. P. (2018). Regio- and diastereoselectivity of the cycloaddition of nitrones with N-propadienylindole and pyrroles. Tetrahedron, 74(1), 174-183. https://doi.org/10.1016/j.tet.2017.11.056

Vancouver

Efremova MM, Novikov AS, Kostikov RR, Panikorovsky TL, Ivanov AV, Molchanov AP. Regio- and diastereoselectivity of the cycloaddition of nitrones with N-propadienylindole and pyrroles. Tetrahedron. 2018 Янв. 4;74(1):174-183. https://doi.org/10.1016/j.tet.2017.11.056

Author

Efremova, M.M. ; Novikov, A.S. ; Kostikov, R.R. ; Panikorovsky, T.L. ; Ivanov, A.V. ; Molchanov, A.P. / Regio- and diastereoselectivity of the cycloaddition of nitrones with N-propadienylindole and pyrroles. в: Tetrahedron. 2018 ; Том 74, № 1. стр. 174-183.

BibTeX

@article{b22701e810b143ad9cb54cef14617264,
title = "Regio- and diastereoselectivity of the cycloaddition of nitrones with N-propadienylindole and pyrroles",
abstract = "The 1,3-dipolar cycloaddition of nitrones to N-propadienyl indoles and pyrroles proceeds predominantly via the C1-C2 bond to form 4-methyleneisoxazolidines. In the case of aldonitrones, the cis-isomers are predominantly formed.",
keywords = "Allenes, Cycloaddition, Isoxazolidines, Nitrones",
author = "M.M. Efremova and A.S. Novikov and R.R. Kostikov and T.L. Panikorovsky and A.V. Ivanov and A.P. Molchanov",
note = "cited By 0",
year = "2018",
month = jan,
day = "4",
doi = "10.1016/j.tet.2017.11.056",
language = "English",
volume = "74",
pages = "174--183",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier",
number = "1",

}

RIS

TY - JOUR

T1 - Regio- and diastereoselectivity of the cycloaddition of nitrones with N-propadienylindole and pyrroles

AU - Efremova, M.M.

AU - Novikov, A.S.

AU - Kostikov, R.R.

AU - Panikorovsky, T.L.

AU - Ivanov, A.V.

AU - Molchanov, A.P.

N1 - cited By 0

PY - 2018/1/4

Y1 - 2018/1/4

N2 - The 1,3-dipolar cycloaddition of nitrones to N-propadienyl indoles and pyrroles proceeds predominantly via the C1-C2 bond to form 4-methyleneisoxazolidines. In the case of aldonitrones, the cis-isomers are predominantly formed.

AB - The 1,3-dipolar cycloaddition of nitrones to N-propadienyl indoles and pyrroles proceeds predominantly via the C1-C2 bond to form 4-methyleneisoxazolidines. In the case of aldonitrones, the cis-isomers are predominantly formed.

KW - Allenes

KW - Cycloaddition

KW - Isoxazolidines

KW - Nitrones

UR - http://www.scopus.com/inward/record.url?scp=85034826652&partnerID=8YFLogxK

U2 - 10.1016/j.tet.2017.11.056

DO - 10.1016/j.tet.2017.11.056

M3 - Article

VL - 74

SP - 174

EP - 183

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 1

ER -

ID: 11475082