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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...

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Detalles Bibliográficos
Autores principales: Beltrá, Jorge, Gimeno, M Concepción, Herrera, Raquel P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
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.
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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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