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[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles. / Efimov, Ilya V.; Matveeva, Maria D.; Luque, Rafael et al.
In: European Journal of Organic Chemistry, Vol. 2020, No. 9, 08.03.2020, p. 1108-1113.

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

Harvard

Efimov, IV, Matveeva, MD, Luque, R, Bakulev, VA & Voskressensky, LG 2020, '[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles', European Journal of Organic Chemistry, vol. 2020, no. 9, pp. 1108-1113. https://doi.org/10.1002/ejoc.201901776

APA

Efimov, I. V., Matveeva, M. D., Luque, R., Bakulev, V. A., & Voskressensky, L. G. (2020). [3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles. European Journal of Organic Chemistry, 2020(9), 1108-1113. https://doi.org/10.1002/ejoc.201901776

Vancouver

Efimov IV, Matveeva MD, Luque R, Bakulev VA, Voskressensky LG. [3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles. European Journal of Organic Chemistry. 2020 Mar 8;2020(9):1108-1113. doi: 10.1002/ejoc.201901776

Author

Efimov, Ilya V. ; Matveeva, Maria D. ; Luque, Rafael et al. / [3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles. In: European Journal of Organic Chemistry. 2020 ; Vol. 2020, No. 9. pp. 1108-1113.

BibTeX

@article{0155801907264a358dc6e0973a247cfe,
title = "[3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles",
keywords = "Cycloaddition, Enamines, Enaminones, Isocyanides, Potassium tert-butoxide, Pyrroles, AZIDES, OLIGOSUBSTITUTED PYRROLES, SUBSTITUTED PYRROLES, CLICK CHEMISTRY, CATALYZED REACTION, ALKYNES, PYRROLE-2-CARBOXYLATES, REGIOSELECTIVE SYNTHESIS, DERIVATIVES, CHLORIN",
author = "Efimov, {Ilya V.} and Matveeva, {Maria D.} and Rafael Luque and Bakulev, {Vasiliy A.} and Voskressensky, {Leonid G.}",
year = "2020",
month = mar,
day = "8",
doi = "10.1002/ejoc.201901776",
language = "English",
volume = "2020",
pages = "1108--1113",
journal = "European Journal of Organic Chemistry",
issn = "1434-193X",
publisher = "Wiley-VCH Verlag",
number = "9",

}

RIS

TY - JOUR

T1 - [3+2] Anionic Cycloaddition of Isocyanides to Acyclic Enamines and Enaminones: A New, Simple, and Convenient Method for the Synthesis of 2,4-Disubstituted Pyrroles

AU - Efimov, Ilya V.

AU - Matveeva, Maria D.

AU - Luque, Rafael

AU - Bakulev, Vasiliy A.

AU - Voskressensky, Leonid G.

PY - 2020/3/8

Y1 - 2020/3/8

KW - Cycloaddition

KW - Enamines

KW - Enaminones

KW - Isocyanides

KW - Potassium tert-butoxide

KW - Pyrroles

KW - AZIDES

KW - OLIGOSUBSTITUTED PYRROLES

KW - SUBSTITUTED PYRROLES

KW - CLICK CHEMISTRY

KW - CATALYZED REACTION

KW - ALKYNES

KW - PYRROLE-2-CARBOXYLATES

KW - REGIOSELECTIVE SYNTHESIS

KW - DERIVATIVES

KW - CHLORIN

UR - http://www.scopus.com/inward/record.url?scp=85079876432&partnerID=8YFLogxK

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000514231100001

U2 - 10.1002/ejoc.201901776

DO - 10.1002/ejoc.201901776

M3 - Article

AN - SCOPUS:85079876432

VL - 2020

SP - 1108

EP - 1113

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

SN - 1434-193X

IS - 9

ER -

ID: 12424074