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Synthesis of Novel 1,4-Naphthoquinones Possessing Indole Scaffolds Using In(OTf)(3) in Solvent-Free Conditions
Novel 1,4-naphthoquinones possessing indole scaffolds were prepared by the reaction of 2-hydroxy-1,4-naphthoquinone-substituted salicylic aldehydes and indoles using In(OTf)(3) as a catalyst. The method has the advantages of simple operation, mild reaction conditions, and friendly environment.
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222671/ https://www.ncbi.nlm.nih.gov/pubmed/30082583 http://dx.doi.org/10.3390/molecules23081954 |
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author | Yang, Xiaojuan Wu, Liqiang |
author_facet | Yang, Xiaojuan Wu, Liqiang |
author_sort | Yang, Xiaojuan |
collection | PubMed |
description | Novel 1,4-naphthoquinones possessing indole scaffolds were prepared by the reaction of 2-hydroxy-1,4-naphthoquinone-substituted salicylic aldehydes and indoles using In(OTf)(3) as a catalyst. The method has the advantages of simple operation, mild reaction conditions, and friendly environment. |
format | Online Article Text |
id | pubmed-6222671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62226712018-11-13 Synthesis of Novel 1,4-Naphthoquinones Possessing Indole Scaffolds Using In(OTf)(3) in Solvent-Free Conditions Yang, Xiaojuan Wu, Liqiang Molecules Article Novel 1,4-naphthoquinones possessing indole scaffolds were prepared by the reaction of 2-hydroxy-1,4-naphthoquinone-substituted salicylic aldehydes and indoles using In(OTf)(3) as a catalyst. The method has the advantages of simple operation, mild reaction conditions, and friendly environment. MDPI 2018-08-06 /pmc/articles/PMC6222671/ /pubmed/30082583 http://dx.doi.org/10.3390/molecules23081954 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yang, Xiaojuan Wu, Liqiang Synthesis of Novel 1,4-Naphthoquinones Possessing Indole Scaffolds Using In(OTf)(3) in Solvent-Free Conditions |
title | Synthesis of Novel 1,4-Naphthoquinones Possessing Indole Scaffolds Using In(OTf)(3) in Solvent-Free Conditions |
title_full | Synthesis of Novel 1,4-Naphthoquinones Possessing Indole Scaffolds Using In(OTf)(3) in Solvent-Free Conditions |
title_fullStr | Synthesis of Novel 1,4-Naphthoquinones Possessing Indole Scaffolds Using In(OTf)(3) in Solvent-Free Conditions |
title_full_unstemmed | Synthesis of Novel 1,4-Naphthoquinones Possessing Indole Scaffolds Using In(OTf)(3) in Solvent-Free Conditions |
title_short | Synthesis of Novel 1,4-Naphthoquinones Possessing Indole Scaffolds Using In(OTf)(3) in Solvent-Free Conditions |
title_sort | synthesis of novel 1,4-naphthoquinones possessing indole scaffolds using in(otf)(3) in solvent-free conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222671/ https://www.ncbi.nlm.nih.gov/pubmed/30082583 http://dx.doi.org/10.3390/molecules23081954 |
work_keys_str_mv | AT yangxiaojuan synthesisofnovel14naphthoquinonespossessingindolescaffoldsusinginotf3insolventfreeconditions AT wuliqiang synthesisofnovel14naphthoquinonespossessingindolescaffoldsusinginotf3insolventfreeconditions |