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A new approach for the synthesis of bisindoles through AgOTf as catalyst
A novel approach for the catalyzed formation of bisindolylmethane derivatives (BIMs) is described. This methodology is the unique example where AgOTf has been successfully used for the activation of aldehydes, giving easy access to a broad range of bisindolyl derivatives with excellent results. More...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168942/ https://www.ncbi.nlm.nih.gov/pubmed/25246979 http://dx.doi.org/10.3762/bjoc.10.228 |
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author | Beltrá, Jorge Gimeno, M Concepción Herrera, Raquel P |
author_facet | Beltrá, Jorge Gimeno, M Concepción Herrera, Raquel P |
author_sort | Beltrá, Jorge |
collection | PubMed |
description | A novel approach for the catalyzed formation of bisindolylmethane derivatives (BIMs) is described. This methodology is the unique example where AgOTf has been successfully used for the activation of aldehydes, giving easy access to a broad range of bisindolyl derivatives with excellent results. Moreover, the simplicity and easy operational methodology using a small amount of commercially available AgOTf (1–3 mol %), one of the lowest catalytic charge used in this process to date, makes this procedure an alternative approach for this interesting and appealing reaction. |
format | Online Article Text |
id | pubmed-4168942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-41689422014-09-22 A new approach for the synthesis of bisindoles through AgOTf as catalyst Beltrá, Jorge Gimeno, M Concepción Herrera, Raquel P Beilstein J Org Chem Full Research Paper A novel approach for the catalyzed formation of bisindolylmethane derivatives (BIMs) is described. This methodology is the unique example where AgOTf has been successfully used for the activation of aldehydes, giving easy access to a broad range of bisindolyl derivatives with excellent results. Moreover, the simplicity and easy operational methodology using a small amount of commercially available AgOTf (1–3 mol %), one of the lowest catalytic charge used in this process to date, makes this procedure an alternative approach for this interesting and appealing reaction. Beilstein-Institut 2014-09-17 /pmc/articles/PMC4168942/ /pubmed/25246979 http://dx.doi.org/10.3762/bjoc.10.228 Text en Copyright © 2014, Beltrá 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 | Full Research Paper Beltrá, Jorge Gimeno, M Concepción Herrera, Raquel P A new approach for the synthesis of bisindoles through AgOTf as catalyst |
title | A new approach for the synthesis of bisindoles through AgOTf as catalyst |
title_full | A new approach for the synthesis of bisindoles through AgOTf as catalyst |
title_fullStr | A new approach for the synthesis of bisindoles through AgOTf as catalyst |
title_full_unstemmed | A new approach for the synthesis of bisindoles through AgOTf as catalyst |
title_short | A new approach for the synthesis of bisindoles through AgOTf as catalyst |
title_sort | new approach for the synthesis of bisindoles through agotf as catalyst |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168942/ https://www.ncbi.nlm.nih.gov/pubmed/25246979 http://dx.doi.org/10.3762/bjoc.10.228 |
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