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Practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst
This paper describes the preparation of indoles, azaindoles and benzofurans in pure water by using a new heterogeneous Pd–Cu/C catalyst through a cascade Sonogashira alkynylation–cyclization sequence. Details of the optimization studies and the substrate scope are discussed. This procedure allows th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3740569/ https://www.ncbi.nlm.nih.gov/pubmed/23946838 http://dx.doi.org/10.3762/bjoc.9.160 |
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author | Rossy, Cybille Fouquet, Eric Felpin, François-Xavier |
author_facet | Rossy, Cybille Fouquet, Eric Felpin, François-Xavier |
author_sort | Rossy, Cybille |
collection | PubMed |
description | This paper describes the preparation of indoles, azaindoles and benzofurans in pure water by using a new heterogeneous Pd–Cu/C catalyst through a cascade Sonogashira alkynylation–cyclization sequence. Details of the optimization studies and the substrate scope are discussed. This procedure allows the preparation of heterocycles with good yields and is tolerant to a wide variety of functional groups. |
format | Online Article Text |
id | pubmed-3740569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-37405692013-08-14 Practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst Rossy, Cybille Fouquet, Eric Felpin, François-Xavier Beilstein J Org Chem Letter This paper describes the preparation of indoles, azaindoles and benzofurans in pure water by using a new heterogeneous Pd–Cu/C catalyst through a cascade Sonogashira alkynylation–cyclization sequence. Details of the optimization studies and the substrate scope are discussed. This procedure allows the preparation of heterocycles with good yields and is tolerant to a wide variety of functional groups. Beilstein-Institut 2013-07-16 /pmc/articles/PMC3740569/ /pubmed/23946838 http://dx.doi.org/10.3762/bjoc.9.160 Text en Copyright © 2013, Rossy et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Letter Rossy, Cybille Fouquet, Eric Felpin, François-Xavier Practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst |
title | Practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst |
title_full | Practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst |
title_fullStr | Practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst |
title_full_unstemmed | Practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst |
title_short | Practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst |
title_sort | practical synthesis of indoles and benzofurans in water using a heterogeneous bimetallic catalyst |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3740569/ https://www.ncbi.nlm.nih.gov/pubmed/23946838 http://dx.doi.org/10.3762/bjoc.9.160 |
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