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Transition metal-free one-pot synthesis of substituted pyrroles by employing aza-Wittig reaction
A mild and metal-free one-pot synthetic strategy has been developed for the construction of substituted pyrroles by employing aza-Wittig reaction from a unique and unexplored combination of chromones and phenacyl azides. This method does not compromise the diverse substitutions on both the phenacyl...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072206/ https://www.ncbi.nlm.nih.gov/pubmed/35529397 http://dx.doi.org/10.1039/c9ra06778g |
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author | Jadala, Chetna Prasad, Budaganaboyina Prasanthi, A. V. G. Shankaraiah, Nagula Kamal, Ahmed |
author_facet | Jadala, Chetna Prasad, Budaganaboyina Prasanthi, A. V. G. Shankaraiah, Nagula Kamal, Ahmed |
author_sort | Jadala, Chetna |
collection | PubMed |
description | A mild and metal-free one-pot synthetic strategy has been developed for the construction of substituted pyrroles by employing aza-Wittig reaction from a unique and unexplored combination of chromones and phenacyl azides. This method does not compromise the diverse substitutions on both the phenacyl azides and chromones. The merits of this method are wide substrate scope, easy functionalization, short reaction time, operationally simple, and higher yields. Moreover, this method is amenable for the generation of a library of key pyrrole building blocks. |
format | Online Article Text |
id | pubmed-9072206 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90722062022-05-06 Transition metal-free one-pot synthesis of substituted pyrroles by employing aza-Wittig reaction Jadala, Chetna Prasad, Budaganaboyina Prasanthi, A. V. G. Shankaraiah, Nagula Kamal, Ahmed RSC Adv Chemistry A mild and metal-free one-pot synthetic strategy has been developed for the construction of substituted pyrroles by employing aza-Wittig reaction from a unique and unexplored combination of chromones and phenacyl azides. This method does not compromise the diverse substitutions on both the phenacyl azides and chromones. The merits of this method are wide substrate scope, easy functionalization, short reaction time, operationally simple, and higher yields. Moreover, this method is amenable for the generation of a library of key pyrrole building blocks. The Royal Society of Chemistry 2019-09-27 /pmc/articles/PMC9072206/ /pubmed/35529397 http://dx.doi.org/10.1039/c9ra06778g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Jadala, Chetna Prasad, Budaganaboyina Prasanthi, A. V. G. Shankaraiah, Nagula Kamal, Ahmed Transition metal-free one-pot synthesis of substituted pyrroles by employing aza-Wittig reaction |
title | Transition metal-free one-pot synthesis of substituted pyrroles by employing aza-Wittig reaction |
title_full | Transition metal-free one-pot synthesis of substituted pyrroles by employing aza-Wittig reaction |
title_fullStr | Transition metal-free one-pot synthesis of substituted pyrroles by employing aza-Wittig reaction |
title_full_unstemmed | Transition metal-free one-pot synthesis of substituted pyrroles by employing aza-Wittig reaction |
title_short | Transition metal-free one-pot synthesis of substituted pyrroles by employing aza-Wittig reaction |
title_sort | transition metal-free one-pot synthesis of substituted pyrroles by employing aza-wittig reaction |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072206/ https://www.ncbi.nlm.nih.gov/pubmed/35529397 http://dx.doi.org/10.1039/c9ra06778g |
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