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Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide
Dess–Martin periodinane (DMP) is a broadly applicable oxidant in chemical synthesis. In this work, an efficient and convenient synthesis of N-substituted isoquinolinone derivatives mediated by DMP was achieved through the oxidative coupling reaction of functionalized isoquinoline with readily availa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919522/ https://www.ncbi.nlm.nih.gov/pubmed/36770590 http://dx.doi.org/10.3390/molecules28030923 |
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author | Yang, Chunmei Zhang, Guoqing Tang, Senling Pan, Yang Shao, Huawu Jiao, Wei |
author_facet | Yang, Chunmei Zhang, Guoqing Tang, Senling Pan, Yang Shao, Huawu Jiao, Wei |
author_sort | Yang, Chunmei |
collection | PubMed |
description | Dess–Martin periodinane (DMP) is a broadly applicable oxidant in chemical synthesis. In this work, an efficient and convenient synthesis of N-substituted isoquinolinone derivatives mediated by DMP was achieved through the oxidative coupling reaction of functionalized isoquinoline with readily available benzyl bromide, which is a metal-free, mild, and practical method for synthesizing isoquinoline-1,3-dione or isoquinoline-1,3,4-trione derivatives in excellent yields. The H(2)O(18)-labeling experiment was performed to gain insight into the possible mechanism for this reaction. |
format | Online Article Text |
id | pubmed-9919522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99195222023-02-12 Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide Yang, Chunmei Zhang, Guoqing Tang, Senling Pan, Yang Shao, Huawu Jiao, Wei Molecules Article Dess–Martin periodinane (DMP) is a broadly applicable oxidant in chemical synthesis. In this work, an efficient and convenient synthesis of N-substituted isoquinolinone derivatives mediated by DMP was achieved through the oxidative coupling reaction of functionalized isoquinoline with readily available benzyl bromide, which is a metal-free, mild, and practical method for synthesizing isoquinoline-1,3-dione or isoquinoline-1,3,4-trione derivatives in excellent yields. The H(2)O(18)-labeling experiment was performed to gain insight into the possible mechanism for this reaction. MDPI 2023-01-17 /pmc/articles/PMC9919522/ /pubmed/36770590 http://dx.doi.org/10.3390/molecules28030923 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yang, Chunmei Zhang, Guoqing Tang, Senling Pan, Yang Shao, Huawu Jiao, Wei Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide |
title | Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide |
title_full | Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide |
title_fullStr | Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide |
title_full_unstemmed | Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide |
title_short | Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide |
title_sort | dess–martin periodinane-mediated oxidative coupling reaction of isoquinoline with benzyl bromide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919522/ https://www.ncbi.nlm.nih.gov/pubmed/36770590 http://dx.doi.org/10.3390/molecules28030923 |
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