DES-Type Interactions To Promote Solvent-Free and Metal-Free Reactions between Nitrogen-Containing Heterocycles and Allylic Alcohols

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Título: DES-Type Interactions To Promote Solvent-Free and Metal-Free Reactions between Nitrogen-Containing Heterocycles and Allylic Alcohols
Autor/es: Martos, Mario | Pérez-Almarcha, Yanira | Pastor, Isidro M.
Grupo/s de investigación o GITE: Alternative Methodologies In Chemistry (AMIC)
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Química Orgánica | Universidad de Alicante. Instituto Universitario de Síntesis Orgánica
Palabras clave: Allylation | Catalysis | DES-type interaction | Nitrogen heterocycles | Sustainable chemistry
Fecha de publicación: 26-oct-2022
Editor: Wiley-VCH GmbH
Cita bibliográfica: European Journal of Organic Chemistry. 2022, 44: e202201221. https://doi.org/10.1002/ejoc.202201221
Resumen: Nitrogen-containing heterocycles are of great interest to organic chemists since they are present in a wide array of bioactive molecules. The use of allylic alcohols to carry out the allylation of heterocycles has been described as a sustainable alternative for this type of functionalization. Among the plethora of methodologies described, the use of metals, solvents, or hazardous reagents is ubiquitous. The protocol described in this work has provided a solventless and metal-free alternative, being mediated by the easy-to-synthesise and reusable 1,3-bis(carboxymethyl)imidazolium chloride. The protocol has resulted compatible with several nitrogen-containing heterocycles (i.e. indole, pyrazole, triazole, tetrazole, carbazole, indazole, and benzotriazole) and allylic alcohols, providing the allylated-heterocycles with up to quantitative yield, being possible to perform the reaction in preparative scale.Based on various green metrics (atom economy, stoichiometric factor, reaction mass efficiency, materials recovery parameter, E-factor, and EcoScale), the overall greenness significance of the methodology has been established.
Patrocinador/es: This work was financially supported by the University of Alicante (VIGROB-316, UADIF20-106, UAUSTI21-15), the Spanish Ministerio de Ciencia, Innovación y Universidades (PGC2018-096616-B-I00), the Spanish Ministerio de Ciencia e Innovación (PID2021-127332NB-I00) and the Generalitat Valenciana (AICO/2021/013). MM thanks the ISO (University of Alicante) for a predoctoral contract.
URI: http://hdl.handle.net/10045/128982
ISSN: 1434-193X (Print) | 1099-0690 (Online)
DOI: 10.1002/ejoc.202201221
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2022 The Authors. European Journal of Organic Chemistry published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Revisión científica: si
Versión del editor: https://doi.org/10.1002/ejoc.202201221
Aparece en las colecciones:INV - AMIC - Artículos de Revistas

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