Cargando…

Development of an imidazole salt catalytic system for the preparation of bis(indolyl)methanes and bis(naphthyl)methane

Imidazolium salts are shown to catalyze the rapid room temperature reaction of indoles or naphthol with aldehydes to provide bis(indolyl)methanes or bis(naphthol)methane in excellent yields and the reaction proceeds optimally in dichloromethane with no base additives. The reaction exhibits a broad s...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xu, Aldrich, Courtney C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483367/
https://www.ncbi.nlm.nih.gov/pubmed/31022274
http://dx.doi.org/10.1371/journal.pone.0216008
_version_ 1783414014767792128
author Wang, Xu
Aldrich, Courtney C.
author_facet Wang, Xu
Aldrich, Courtney C.
author_sort Wang, Xu
collection PubMed
description Imidazolium salts are shown to catalyze the rapid room temperature reaction of indoles or naphthol with aldehydes to provide bis(indolyl)methanes or bis(naphthol)methane in excellent yields and the reaction proceeds optimally in dichloromethane with no base additives. The reaction exhibits a broad substrate tolerance and occurs through nucleophilic activation of the indoles and naphthols through a cation–π interaction.
format Online
Article
Text
id pubmed-6483367
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-64833672019-05-09 Development of an imidazole salt catalytic system for the preparation of bis(indolyl)methanes and bis(naphthyl)methane Wang, Xu Aldrich, Courtney C. PLoS One Research Article Imidazolium salts are shown to catalyze the rapid room temperature reaction of indoles or naphthol with aldehydes to provide bis(indolyl)methanes or bis(naphthol)methane in excellent yields and the reaction proceeds optimally in dichloromethane with no base additives. The reaction exhibits a broad substrate tolerance and occurs through nucleophilic activation of the indoles and naphthols through a cation–π interaction. Public Library of Science 2019-04-25 /pmc/articles/PMC6483367/ /pubmed/31022274 http://dx.doi.org/10.1371/journal.pone.0216008 Text en © 2019 Wang, Aldrich http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Xu
Aldrich, Courtney C.
Development of an imidazole salt catalytic system for the preparation of bis(indolyl)methanes and bis(naphthyl)methane
title Development of an imidazole salt catalytic system for the preparation of bis(indolyl)methanes and bis(naphthyl)methane
title_full Development of an imidazole salt catalytic system for the preparation of bis(indolyl)methanes and bis(naphthyl)methane
title_fullStr Development of an imidazole salt catalytic system for the preparation of bis(indolyl)methanes and bis(naphthyl)methane
title_full_unstemmed Development of an imidazole salt catalytic system for the preparation of bis(indolyl)methanes and bis(naphthyl)methane
title_short Development of an imidazole salt catalytic system for the preparation of bis(indolyl)methanes and bis(naphthyl)methane
title_sort development of an imidazole salt catalytic system for the preparation of bis(indolyl)methanes and bis(naphthyl)methane
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483367/
https://www.ncbi.nlm.nih.gov/pubmed/31022274
http://dx.doi.org/10.1371/journal.pone.0216008
work_keys_str_mv AT wangxu developmentofanimidazolesaltcatalyticsystemforthepreparationofbisindolylmethanesandbisnaphthylmethane
AT aldrichcourtneyc developmentofanimidazolesaltcatalyticsystemforthepreparationofbisindolylmethanesandbisnaphthylmethane