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...
Autores principales: | , |
---|---|
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 |