[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-Reference-Cited by-同舟云学术

[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

Published:2020-02-19 Issue:9 Volume:2020 Page:1108-1113
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Efimov Ilya V.¹,Matveeva Maria D.¹,Luque Rafael¹²^ORCID,Bakulev Vasiliy A.³,Voskressensky Leonid G.¹

Affiliation:

1. Research Center: Molecular Design and Synthesis of Innovative Compounds for Medicine; Peoples' Friendship University of Russia (RUDN University); Miklukho-Maklaya st, 6 117198 Moscow Russia

2. Departamento de Quimica Organica, Universidad de Cordoba; Campus de Rabanales, Edificio Marie Curie (C-3); Universidad de Cordoba; Ctra Nnal IV-A, Km 396 Cordoba Spain

3. Campus de Rabanales, Edificio Marie Curie (C-3); Ural Federal University named after the first President of Russia B. N. Yeltsin; 19 Mira st. 620002 Yekaterinburg Russia

Funder

RUDN UNiversity

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201901776/fullpdf

Reference56 articles.

1. Isoxazoles

2. Click Chemistry - What’s in a Name? Triazole Synthesis and Beyond

3. 1,2,3-Triazole-containing hybrids as leads in medicinal chemistry: A recent overview

4. Recent applications of click chemistry in drug discovery

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