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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...

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Autores principales: Chen, Rongxiang, Liu, Bing, Li, Wenbo, Wang, Kai-Kai, Miao, Changqing, Li, Zhizhuang, Lv, Yingjie, Liu, Lantao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
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.
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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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