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Domino transformation of isoxazoles to 2,4-dicarbonylpyrroles under Fe/Ni relay catalysis. / Galenko, E.E.; Galenko, A.V.; Khlebnikov, A.F.; Novikov, M.S.

In: RSC Advances, Vol. 5, 2015, p. 18172-18176.

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

Harvard

Galenko, EE, Galenko, AV, Khlebnikov, AF & Novikov, MS 2015, 'Domino transformation of isoxazoles to 2,4-dicarbonylpyrroles under Fe/Ni relay catalysis', RSC Advances, vol. 5, pp. 18172-18176. https://doi.org/10.1039/c5ra01889g

APA

Galenko, E. E., Galenko, A. V., Khlebnikov, A. F., & Novikov, M. S. (2015). Domino transformation of isoxazoles to 2,4-dicarbonylpyrroles under Fe/Ni relay catalysis. RSC Advances, 5, 18172-18176. https://doi.org/10.1039/c5ra01889g

Vancouver

Galenko EE, Galenko AV, Khlebnikov AF, Novikov MS. Domino transformation of isoxazoles to 2,4-dicarbonylpyrroles under Fe/Ni relay catalysis. RSC Advances. 2015;5:18172-18176. https://doi.org/10.1039/c5ra01889g

Author

Galenko, E.E. ; Galenko, A.V. ; Khlebnikov, A.F. ; Novikov, M.S. / Domino transformation of isoxazoles to 2,4-dicarbonylpyrroles under Fe/Ni relay catalysis. In: RSC Advances. 2015 ; Vol. 5. pp. 18172-18176.

BibTeX

@article{02a61a7b763744139b72508566715eb9,
title = "Domino transformation of isoxazoles to 2,4-dicarbonylpyrroles under Fe/Ni relay catalysis",
abstract = "The domino reaction of 5-alkoxy- or 5-aminoisoxazoles, under metal relay catalysis, with symmetric 1,3-diketones gives 4-acylpyrrole-2- carboxylic acid derivatives in high yield. Esters and amides of acylacetic acids react regioselectively, giving derivatives of pyrrole-2,4-dicarboxylic acid as the main products.",
author = "E.E. Galenko and A.V. Galenko and A.F. Khlebnikov and M.S. Novikov",
year = "2015",
doi = "10.1039/c5ra01889g",
language = "English",
volume = "5",
pages = "18172--18176",
journal = "RSC Advances",
issn = "2046-2069",
publisher = "Royal Society of Chemistry",

}

RIS

TY - JOUR

T1 - Domino transformation of isoxazoles to 2,4-dicarbonylpyrroles under Fe/Ni relay catalysis

AU - Galenko, E.E.

AU - Galenko, A.V.

AU - Khlebnikov, A.F.

AU - Novikov, M.S.

PY - 2015

Y1 - 2015

N2 - The domino reaction of 5-alkoxy- or 5-aminoisoxazoles, under metal relay catalysis, with symmetric 1,3-diketones gives 4-acylpyrrole-2- carboxylic acid derivatives in high yield. Esters and amides of acylacetic acids react regioselectively, giving derivatives of pyrrole-2,4-dicarboxylic acid as the main products.

AB - The domino reaction of 5-alkoxy- or 5-aminoisoxazoles, under metal relay catalysis, with symmetric 1,3-diketones gives 4-acylpyrrole-2- carboxylic acid derivatives in high yield. Esters and amides of acylacetic acids react regioselectively, giving derivatives of pyrrole-2,4-dicarboxylic acid as the main products.

U2 - 10.1039/c5ra01889g

DO - 10.1039/c5ra01889g

M3 - Article

VL - 5

SP - 18172

EP - 18176

JO - RSC Advances

JF - RSC Advances

SN - 2046-2069

ER -

ID: 3926744