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Metal-free oxidative coupling of arylmethylamines with indoles: a simple, environmentally benign approach for the synthesis of 3,3′-bis(indolyl)methanes

The efficient metal-free oxidative coupling of arylmethylamines with indoles has been developed using molecular oxygen as a green oxidant. The present reaction provides a novel route towards the synthesis of 3,3′-bis(indolyl)methanes in excellent yields of up to 95% via C–C and C–N bond formation. T...

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Detalles Bibliográficos
Autores principales: Kadu, Vikas D., Chandrudu, Sankala Naga, Hublikar, Mahesh G., Raut, Dattatraya G., Bhosale, Raghunath B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054727/
https://www.ncbi.nlm.nih.gov/pubmed/35520337
http://dx.doi.org/10.1039/d0ra03221b
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author Kadu, Vikas D.
Chandrudu, Sankala Naga
Hublikar, Mahesh G.
Raut, Dattatraya G.
Bhosale, Raghunath B.
author_facet Kadu, Vikas D.
Chandrudu, Sankala Naga
Hublikar, Mahesh G.
Raut, Dattatraya G.
Bhosale, Raghunath B.
author_sort Kadu, Vikas D.
collection PubMed
description The efficient metal-free oxidative coupling of arylmethylamines with indoles has been developed using molecular oxygen as a green oxidant. The present reaction provides a novel route towards the synthesis of 3,3′-bis(indolyl)methanes in excellent yields of up to 95% via C–C and C–N bond formation. This attractive and environmentally friendly one-pot protocol is a simple procedure that features inexpensive acetic acid as the catalyst and molecular oxygen as the sole oxidant, and it supports a wide substrate scope with the good tolerance of functional groups.
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spelling pubmed-90547272022-05-04 Metal-free oxidative coupling of arylmethylamines with indoles: a simple, environmentally benign approach for the synthesis of 3,3′-bis(indolyl)methanes Kadu, Vikas D. Chandrudu, Sankala Naga Hublikar, Mahesh G. Raut, Dattatraya G. Bhosale, Raghunath B. RSC Adv Chemistry The efficient metal-free oxidative coupling of arylmethylamines with indoles has been developed using molecular oxygen as a green oxidant. The present reaction provides a novel route towards the synthesis of 3,3′-bis(indolyl)methanes in excellent yields of up to 95% via C–C and C–N bond formation. This attractive and environmentally friendly one-pot protocol is a simple procedure that features inexpensive acetic acid as the catalyst and molecular oxygen as the sole oxidant, and it supports a wide substrate scope with the good tolerance of functional groups. The Royal Society of Chemistry 2020-06-17 /pmc/articles/PMC9054727/ /pubmed/35520337 http://dx.doi.org/10.1039/d0ra03221b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kadu, Vikas D.
Chandrudu, Sankala Naga
Hublikar, Mahesh G.
Raut, Dattatraya G.
Bhosale, Raghunath B.
Metal-free oxidative coupling of arylmethylamines with indoles: a simple, environmentally benign approach for the synthesis of 3,3′-bis(indolyl)methanes
title Metal-free oxidative coupling of arylmethylamines with indoles: a simple, environmentally benign approach for the synthesis of 3,3′-bis(indolyl)methanes
title_full Metal-free oxidative coupling of arylmethylamines with indoles: a simple, environmentally benign approach for the synthesis of 3,3′-bis(indolyl)methanes
title_fullStr Metal-free oxidative coupling of arylmethylamines with indoles: a simple, environmentally benign approach for the synthesis of 3,3′-bis(indolyl)methanes
title_full_unstemmed Metal-free oxidative coupling of arylmethylamines with indoles: a simple, environmentally benign approach for the synthesis of 3,3′-bis(indolyl)methanes
title_short Metal-free oxidative coupling of arylmethylamines with indoles: a simple, environmentally benign approach for the synthesis of 3,3′-bis(indolyl)methanes
title_sort metal-free oxidative coupling of arylmethylamines with indoles: a simple, environmentally benign approach for the synthesis of 3,3′-bis(indolyl)methanes
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054727/
https://www.ncbi.nlm.nih.gov/pubmed/35520337
http://dx.doi.org/10.1039/d0ra03221b
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