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Metal-free C–H arylation of imidazoheterocycles with aryl hydrazines
A simple and efficient metal-free arylation of imidazo[1,2-a]pyridines at the C-3 position with arylhydrazine has been achieved at room temperature under ambient air conditions. Various 2,3-disubstituted imidazopyridines and imidazothiazoles were synthesized with high yields. The present methodology...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079221/ https://www.ncbi.nlm.nih.gov/pubmed/35539413 http://dx.doi.org/10.1039/c8ra01474d |
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author | Jana, Sourav Samanta, Sadhanendu Bagdi, Avik K. Shirinian, Valerii Z. Hajra, Alakananda |
author_facet | Jana, Sourav Samanta, Sadhanendu Bagdi, Avik K. Shirinian, Valerii Z. Hajra, Alakananda |
author_sort | Jana, Sourav |
collection | PubMed |
description | A simple and efficient metal-free arylation of imidazo[1,2-a]pyridines at the C-3 position with arylhydrazine has been achieved at room temperature under ambient air conditions. Various 2,3-disubstituted imidazopyridines and imidazothiazoles were synthesized with high yields. The present methodology demonstrates the usefulness of commercially available aryl hydrazine as an arylating agent. |
format | Online Article Text |
id | pubmed-9079221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90792212022-05-09 Metal-free C–H arylation of imidazoheterocycles with aryl hydrazines Jana, Sourav Samanta, Sadhanendu Bagdi, Avik K. Shirinian, Valerii Z. Hajra, Alakananda RSC Adv Chemistry A simple and efficient metal-free arylation of imidazo[1,2-a]pyridines at the C-3 position with arylhydrazine has been achieved at room temperature under ambient air conditions. Various 2,3-disubstituted imidazopyridines and imidazothiazoles were synthesized with high yields. The present methodology demonstrates the usefulness of commercially available aryl hydrazine as an arylating agent. The Royal Society of Chemistry 2018-04-03 /pmc/articles/PMC9079221/ /pubmed/35539413 http://dx.doi.org/10.1039/c8ra01474d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Jana, Sourav Samanta, Sadhanendu Bagdi, Avik K. Shirinian, Valerii Z. Hajra, Alakananda Metal-free C–H arylation of imidazoheterocycles with aryl hydrazines |
title | Metal-free C–H arylation of imidazoheterocycles with aryl hydrazines |
title_full | Metal-free C–H arylation of imidazoheterocycles with aryl hydrazines |
title_fullStr | Metal-free C–H arylation of imidazoheterocycles with aryl hydrazines |
title_full_unstemmed | Metal-free C–H arylation of imidazoheterocycles with aryl hydrazines |
title_short | Metal-free C–H arylation of imidazoheterocycles with aryl hydrazines |
title_sort | metal-free c–h arylation of imidazoheterocycles with aryl hydrazines |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079221/ https://www.ncbi.nlm.nih.gov/pubmed/35539413 http://dx.doi.org/10.1039/c8ra01474d |
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