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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...

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Detalles Bibliográficos
Autores principales: Jadala, Chetna, Prasad, Budaganaboyina, Prasanthi, A. V. G., Shankaraiah, Nagula, Kamal, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
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.
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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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