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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...

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Detalles Bibliográficos
Autores principales: Yang, Chunmei, Zhang, Guoqing, Tang, Senling, Pan, Yang, Shao, Huawu, Jiao, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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