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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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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. |
format | Online Article Text |
id | pubmed-7057683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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