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Synthesis of 4-Hydroxycarbazole Derivatives by Benzannulation of 3-Nitroindoles with Alkylidene Azlactones

[Image: see text] A general synthesis of 4-hydroxylcarbazoles by domino vinylogous conjugate addition/cyclization/elimination/aromatization of easily prepared 3-nitroindoles with alkylidene azlactones under mild and transition-metal-free conditions has been developed. This method was also applicable...

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Autores principales: Cao, Dongdong, Chen, Gang, Chen, Dingben, Xia, Zhijun, Li, Zongyang, Wang, Yi, Xu, Dongqing, Yang, Jianguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264937/
https://www.ncbi.nlm.nih.gov/pubmed/34250355
http://dx.doi.org/10.1021/acsomega.1c01992
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author Cao, Dongdong
Chen, Gang
Chen, Dingben
Xia, Zhijun
Li, Zongyang
Wang, Yi
Xu, Dongqing
Yang, Jianguo
author_facet Cao, Dongdong
Chen, Gang
Chen, Dingben
Xia, Zhijun
Li, Zongyang
Wang, Yi
Xu, Dongqing
Yang, Jianguo
author_sort Cao, Dongdong
collection PubMed
description [Image: see text] A general synthesis of 4-hydroxylcarbazoles by domino vinylogous conjugate addition/cyclization/elimination/aromatization of easily prepared 3-nitroindoles with alkylidene azlactones under mild and transition-metal-free conditions has been developed. This method was also applicable to other nitrosubstituted benzofused heterocycles such as 3-nitrobenzothiophene, 2-nitrobenzothiophene, and 2-nitrobenzofuran. The valuable tetracyclic carbazole derivatives, such as 6H-oxazolo[4,5-c]carbazole and 3,6-dihydro-2H-oxazolo[4,5-c]carbazol-2-one, were readily prepared from the product, demonstrating synthetic utility of this method.
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spelling pubmed-82649372021-07-09 Synthesis of 4-Hydroxycarbazole Derivatives by Benzannulation of 3-Nitroindoles with Alkylidene Azlactones Cao, Dongdong Chen, Gang Chen, Dingben Xia, Zhijun Li, Zongyang Wang, Yi Xu, Dongqing Yang, Jianguo ACS Omega [Image: see text] A general synthesis of 4-hydroxylcarbazoles by domino vinylogous conjugate addition/cyclization/elimination/aromatization of easily prepared 3-nitroindoles with alkylidene azlactones under mild and transition-metal-free conditions has been developed. This method was also applicable to other nitrosubstituted benzofused heterocycles such as 3-nitrobenzothiophene, 2-nitrobenzothiophene, and 2-nitrobenzofuran. The valuable tetracyclic carbazole derivatives, such as 6H-oxazolo[4,5-c]carbazole and 3,6-dihydro-2H-oxazolo[4,5-c]carbazol-2-one, were readily prepared from the product, demonstrating synthetic utility of this method. American Chemical Society 2021-06-25 /pmc/articles/PMC8264937/ /pubmed/34250355 http://dx.doi.org/10.1021/acsomega.1c01992 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Cao, Dongdong
Chen, Gang
Chen, Dingben
Xia, Zhijun
Li, Zongyang
Wang, Yi
Xu, Dongqing
Yang, Jianguo
Synthesis of 4-Hydroxycarbazole Derivatives by Benzannulation of 3-Nitroindoles with Alkylidene Azlactones
title Synthesis of 4-Hydroxycarbazole Derivatives by Benzannulation of 3-Nitroindoles with Alkylidene Azlactones
title_full Synthesis of 4-Hydroxycarbazole Derivatives by Benzannulation of 3-Nitroindoles with Alkylidene Azlactones
title_fullStr Synthesis of 4-Hydroxycarbazole Derivatives by Benzannulation of 3-Nitroindoles with Alkylidene Azlactones
title_full_unstemmed Synthesis of 4-Hydroxycarbazole Derivatives by Benzannulation of 3-Nitroindoles with Alkylidene Azlactones
title_short Synthesis of 4-Hydroxycarbazole Derivatives by Benzannulation of 3-Nitroindoles with Alkylidene Azlactones
title_sort synthesis of 4-hydroxycarbazole derivatives by benzannulation of 3-nitroindoles with alkylidene azlactones
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264937/
https://www.ncbi.nlm.nih.gov/pubmed/34250355
http://dx.doi.org/10.1021/acsomega.1c01992
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