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Synthesis of N-alkoxyphthalimide derivatives via PIDA-promoted cross dehydrogenative coupling reaction
A PIDA-promoted cross-dehydrogenative coupling reaction between N-hydroxyphthalimide (NHPI) and aryl ketones for efficient synthesis of N-alkoxyphthalimide products in moderate to good yields has been described. This methodology is distinguished by catalyst-free conditions, readily available startin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695068/ https://www.ncbi.nlm.nih.gov/pubmed/35423297 http://dx.doi.org/10.1039/d1ra00375e |
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author | Chen, Rongxiang Liu, Bing Li, Wenbo Wang, Kai-Kai Miao, Changqing Li, Zhizhuang Lv, Yingjie Liu, Lantao |
author_facet | Chen, Rongxiang Liu, Bing Li, Wenbo Wang, Kai-Kai Miao, Changqing Li, Zhizhuang Lv, Yingjie Liu, Lantao |
author_sort | Chen, Rongxiang |
collection | PubMed |
description | A PIDA-promoted cross-dehydrogenative coupling reaction between N-hydroxyphthalimide (NHPI) and aryl ketones for efficient synthesis of N-alkoxyphthalimide products in moderate to good yields has been described. This methodology is distinguished by catalyst-free conditions, readily available starting materials, wide substrate scope and operational simplicity. In addition, a gram-scale reaction and synthetic transformation of the product into synthetically useful intermediates has been demonstrated. |
format | Online Article Text |
id | pubmed-8695068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86950682022-04-13 Synthesis of N-alkoxyphthalimide derivatives via PIDA-promoted cross dehydrogenative coupling reaction Chen, Rongxiang Liu, Bing Li, Wenbo Wang, Kai-Kai Miao, Changqing Li, Zhizhuang Lv, Yingjie Liu, Lantao RSC Adv Chemistry A PIDA-promoted cross-dehydrogenative coupling reaction between N-hydroxyphthalimide (NHPI) and aryl ketones for efficient synthesis of N-alkoxyphthalimide products in moderate to good yields has been described. This methodology is distinguished by catalyst-free conditions, readily available starting materials, wide substrate scope and operational simplicity. In addition, a gram-scale reaction and synthetic transformation of the product into synthetically useful intermediates has been demonstrated. The Royal Society of Chemistry 2021-02-19 /pmc/articles/PMC8695068/ /pubmed/35423297 http://dx.doi.org/10.1039/d1ra00375e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Chen, Rongxiang Liu, Bing Li, Wenbo Wang, Kai-Kai Miao, Changqing Li, Zhizhuang Lv, Yingjie Liu, Lantao Synthesis of N-alkoxyphthalimide derivatives via PIDA-promoted cross dehydrogenative coupling reaction |
title | Synthesis of N-alkoxyphthalimide derivatives via PIDA-promoted cross dehydrogenative coupling reaction |
title_full | Synthesis of N-alkoxyphthalimide derivatives via PIDA-promoted cross dehydrogenative coupling reaction |
title_fullStr | Synthesis of N-alkoxyphthalimide derivatives via PIDA-promoted cross dehydrogenative coupling reaction |
title_full_unstemmed | Synthesis of N-alkoxyphthalimide derivatives via PIDA-promoted cross dehydrogenative coupling reaction |
title_short | Synthesis of N-alkoxyphthalimide derivatives via PIDA-promoted cross dehydrogenative coupling reaction |
title_sort | synthesis of n-alkoxyphthalimide derivatives via pida-promoted cross dehydrogenative coupling reaction |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695068/ https://www.ncbi.nlm.nih.gov/pubmed/35423297 http://dx.doi.org/10.1039/d1ra00375e |
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