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Multicomponent Reactions (MCRs)

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Organic Chemistry".

Deadline for manuscript submissions: closed (31 August 2022) | Viewed by 2659

Special Issue Editor


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Guest Editor
Department of Chemistry in Pharmaceutical Sciences, Faculty of Pharmacy, Complutense University, 28040 Madrid, Spain
Interests: drug development; green chemistry; mechanochemistry; heterocycle synthesis; Alzheimer's disease
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

A popular definition of multicomponent reactions (MCRs) in the scientific community is: "MCRs are a convergent reaction class, in which three or more commercially available or simple molecules react to contribute significantly, with all or many of their atoms, to the final reaction product". MCRs proceed as a one-pot reaction through either a single reaction step or through sequential steps (without the need to replace the reaction medium), followed by a reaction cascade or equilibrium in which different atoms are assembled, leading to the final product.

MCRs have long been studied, such as the Strecker reaction in 1850 and the synthesis of dihydropyridines by Hantzsch in 1890, among others. However, it was early in this century that MCRs showed remarkable progress as a powerful and versatile tool for combatting modern synthesis challenges such as diversity-oriented synthesis (DOS), green chemistry, and combinatorial chemistry. In this context, different areas of organic synthesis have explored multicomponent reactions, with special emphasis on the development of compounds with a wide range of biological activities.

This Special Issue will present original research using MCRs or in which new MCRs will be developed.

Prof. Dr. Juan F. González
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Molecules is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • multicomponent reactions
  • sequential reactions
  • synthetic strategies
  • green chemistry
  • chemical space
  • diversity-oriented synthesis

Published Papers (1 paper)

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Research

10 pages, 1385 KiB  
Article
Piperidine-Iodine as Efficient Dual Catalyst for the One-Pot, Three-Component Synthesis of Coumarin-3-Carboxamides
by Manuel Velasco, Nancy Romero-Ceronio, Rosalía Torralba, Oswaldo Hernández Abreu, Miguel A. Vilchis-Reyes, Erika Alarcón-Matus, Erika M. Ramos-Rivera, David M. Aparicio, Jacqueline Jiménez, Eric Aguilar García, David Cruz Cruz, Clarisa Villegas Gómez and Cuauhtémoc Alvarado
Molecules 2022, 27(14), 4659; https://doi.org/10.3390/molecules27144659 - 21 Jul 2022
Cited by 3 | Viewed by 2323
Abstract
A simple and efficient one-pot, three-component synthetic method for the preparation of coumarin-3-carboxamides was carried out by the reaction of salicylaldehyde, aliphatic primary/secondary amines, and diethylmalonate. The protocol employs piperidine-iodine as a dual system catalyst and ethanol, a green solvent. The main advantages [...] Read more.
A simple and efficient one-pot, three-component synthetic method for the preparation of coumarin-3-carboxamides was carried out by the reaction of salicylaldehyde, aliphatic primary/secondary amines, and diethylmalonate. The protocol employs piperidine-iodine as a dual system catalyst and ethanol, a green solvent. The main advantages of this approach are that it is a metal-free and clean reaction, has low catalyst loading, and requires no tedious workup. Full article
(This article belongs to the Special Issue Multicomponent Reactions (MCRs))
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