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Generation of Aryl Radicals from Aryl Hydrazines via Catalytic Iodine in Air: Arylation of Substituted 1,4-Naphthoquinones

[Image: see text] Arylated building blocks or heterocycles are key to myriad applications, including pharmaceutical drug discovery, materials sciences, and many more. Herein, we have reported a mild and efficient strategy for generation of aryl radicals by reacting appropriate aryl hydrazines with c...

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Autores principales: Sar, Saibal, Chauhan, Jyoti, Sen, Subhabrata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057683/
https://www.ncbi.nlm.nih.gov/pubmed/32149251
http://dx.doi.org/10.1021/acsomega.9b04014
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author Sar, Saibal
Chauhan, Jyoti
Sen, Subhabrata
author_facet Sar, Saibal
Chauhan, Jyoti
Sen, Subhabrata
author_sort Sar, Saibal
collection PubMed
description [Image: see text] Arylated building blocks or heterocycles are key to myriad applications, including pharmaceutical drug discovery, materials sciences, and many more. Herein, we have reported a mild and efficient strategy for generation of aryl radicals by reacting appropriate aryl hydrazines with catalytic iodine in open air. The aryl radicals were quenched by diversely substituted 1,4-napthoquinones present in the reaction mixture to afford diversely substituted 2,3-napthoquinones in moderate to excellent yield. Control experiments provided insights into the putative reaction mechanism.
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spelling pubmed-70576832020-03-06 Generation of Aryl Radicals from Aryl Hydrazines via Catalytic Iodine in Air: Arylation of Substituted 1,4-Naphthoquinones Sar, Saibal Chauhan, Jyoti Sen, Subhabrata ACS Omega [Image: see text] Arylated building blocks or heterocycles are key to myriad applications, including pharmaceutical drug discovery, materials sciences, and many more. Herein, we have reported a mild and efficient strategy for generation of aryl radicals by reacting appropriate aryl hydrazines with catalytic iodine in open air. The aryl radicals were quenched by diversely substituted 1,4-napthoquinones present in the reaction mixture to afford diversely substituted 2,3-napthoquinones in moderate to excellent yield. Control experiments provided insights into the putative reaction mechanism. American Chemical Society 2020-02-21 /pmc/articles/PMC7057683/ /pubmed/32149251 http://dx.doi.org/10.1021/acsomega.9b04014 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Sar, Saibal
Chauhan, Jyoti
Sen, Subhabrata
Generation of Aryl Radicals from Aryl Hydrazines via Catalytic Iodine in Air: Arylation of Substituted 1,4-Naphthoquinones
title Generation of Aryl Radicals from Aryl Hydrazines via Catalytic Iodine in Air: Arylation of Substituted 1,4-Naphthoquinones
title_full Generation of Aryl Radicals from Aryl Hydrazines via Catalytic Iodine in Air: Arylation of Substituted 1,4-Naphthoquinones
title_fullStr Generation of Aryl Radicals from Aryl Hydrazines via Catalytic Iodine in Air: Arylation of Substituted 1,4-Naphthoquinones
title_full_unstemmed Generation of Aryl Radicals from Aryl Hydrazines via Catalytic Iodine in Air: Arylation of Substituted 1,4-Naphthoquinones
title_short Generation of Aryl Radicals from Aryl Hydrazines via Catalytic Iodine in Air: Arylation of Substituted 1,4-Naphthoquinones
title_sort generation of aryl radicals from aryl hydrazines via catalytic iodine in air: arylation of substituted 1,4-naphthoquinones
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057683/
https://www.ncbi.nlm.nih.gov/pubmed/32149251
http://dx.doi.org/10.1021/acsomega.9b04014
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