2-Imidazolidinone benzofurans as unexpected outcome of the Lewis acid mediated Nenitzescu reaction-Reference-Cited by-同舟云学术

2-Imidazolidinone benzofurans as unexpected outcome of the Lewis acid mediated Nenitzescu reaction

Published:2022 Issue:5 Volume:46 Page:2028-2032
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Horsten Tomas¹^ORCID,Alegbejo Price Temitayo Omowumi²^ORCID,Van Meervelt Luc³^ORCID,Emery Flavio da Silva²^ORCID,Dehaen Wim¹^ORCID

Affiliation:

1. Molecular Design and Synthesis, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Leuven 3001, Belgium

2. Department of Pharmaceutical Sciences, School of Pharmaceutical Sciences at Ribeirao Preto of the University of Sao Paulo, Ribeirao Preto, SP, 14040-903, Brazil

3. Biochemistry, Molecular and Structural Biology Section, Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Leuven 3001, Belgium

Abstract

Herein, a metal-free methodology towards 2-imidazolidinone benzofurans via piperazinone enaminoesters addition onto quinones and subsequent rearrangement has been disclosed.

Funder

KU Leuven

Hercules Foundation

Fundação de Amparo à Pesquisa do Estado de São Paulo

Fonds Wetenschappelijk Onderzoek

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D1NJ04965H

Reference51 articles.

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2. Synthesis, biological activity, and evaluation of the mode of action of novel antitubercular benzofurobenzopyrans substituted on A ring

3. Application of the Meerwein reaction of 1,4-benzoquinone to a metal-free synthesis of benzofuropyridine analogues

4. Tandem Nenitzescu Reaction/Nucleophilic Aromatic Substitution to Form Novel Pyrido Fused Indole Frameworks

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