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Facile synthesis of indolo[3,2-a]carbazoles via Pd-catalyzed twofold oxidative cyclization
A rapid and efficient route has been developed for the synthesis of 9-methoxycarbonylindolo[3,2-a]carbazole derivatives. The key steps in this approach involved an aromatic amination and an oxidative biaryl coupling. Via the present route, indolo[3,2-a]carbazole derivatives are available in 3–4 step...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238593/ https://www.ncbi.nlm.nih.gov/pubmed/28144317 http://dx.doi.org/10.3762/bjoc.12.243 |
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author | Yang, Chao Lin, Kai Huang, Lan Pan, Wei-dong Liu, Sheng |
author_facet | Yang, Chao Lin, Kai Huang, Lan Pan, Wei-dong Liu, Sheng |
author_sort | Yang, Chao |
collection | PubMed |
description | A rapid and efficient route has been developed for the synthesis of 9-methoxycarbonylindolo[3,2-a]carbazole derivatives. The key steps in this approach involved an aromatic amination and an oxidative biaryl coupling. Via the present route, indolo[3,2-a]carbazole derivatives are available in 3–4 steps based on commercially available starting materials. |
format | Online Article Text |
id | pubmed-5238593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-52385932017-01-31 Facile synthesis of indolo[3,2-a]carbazoles via Pd-catalyzed twofold oxidative cyclization Yang, Chao Lin, Kai Huang, Lan Pan, Wei-dong Liu, Sheng Beilstein J Org Chem Letter A rapid and efficient route has been developed for the synthesis of 9-methoxycarbonylindolo[3,2-a]carbazole derivatives. The key steps in this approach involved an aromatic amination and an oxidative biaryl coupling. Via the present route, indolo[3,2-a]carbazole derivatives are available in 3–4 steps based on commercially available starting materials. Beilstein-Institut 2016-11-22 /pmc/articles/PMC5238593/ /pubmed/28144317 http://dx.doi.org/10.3762/bjoc.12.243 Text en Copyright © 2016, Yang et al. https://creativecommons.org/licenses/by/4.0https://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/4.0), 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 Yang, Chao Lin, Kai Huang, Lan Pan, Wei-dong Liu, Sheng Facile synthesis of indolo[3,2-a]carbazoles via Pd-catalyzed twofold oxidative cyclization |
title | Facile synthesis of indolo[3,2-a]carbazoles via Pd-catalyzed twofold oxidative cyclization |
title_full | Facile synthesis of indolo[3,2-a]carbazoles via Pd-catalyzed twofold oxidative cyclization |
title_fullStr | Facile synthesis of indolo[3,2-a]carbazoles via Pd-catalyzed twofold oxidative cyclization |
title_full_unstemmed | Facile synthesis of indolo[3,2-a]carbazoles via Pd-catalyzed twofold oxidative cyclization |
title_short | Facile synthesis of indolo[3,2-a]carbazoles via Pd-catalyzed twofold oxidative cyclization |
title_sort | facile synthesis of indolo[3,2-a]carbazoles via pd-catalyzed twofold oxidative cyclization |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238593/ https://www.ncbi.nlm.nih.gov/pubmed/28144317 http://dx.doi.org/10.3762/bjoc.12.243 |
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