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Ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2)
The first ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2) to generate important aryl acetic acids is reported. Besides aldehyde hydrazones, a variety of ketone hydrazones, which have not been successfully applied in previous umpolung reactions with other reactive electrophiles, a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5982211/ https://www.ncbi.nlm.nih.gov/pubmed/29910940 http://dx.doi.org/10.1039/c8sc01299g |
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author | Yan, Si-Shun Zhu, Lei Ye, Jian-Heng Zhang, Zhen Huang, He Zeng, Huiying Li, Chao-Jun Lan, Yu Yu, Da-Gang |
author_facet | Yan, Si-Shun Zhu, Lei Ye, Jian-Heng Zhang, Zhen Huang, He Zeng, Huiying Li, Chao-Jun Lan, Yu Yu, Da-Gang |
author_sort | Yan, Si-Shun |
collection | PubMed |
description | The first ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2) to generate important aryl acetic acids is reported. Besides aldehyde hydrazones, a variety of ketone hydrazones, which have not been successfully applied in previous umpolung reactions with other reactive electrophiles, also show high reactivity and selectivity under mild conditions. Moreover, this operationally simple protocol features good functional group tolerance, is readily scalable, and offers easy derivation of important structures, including bioactive felbinac and adiphenine. Computational studies reveal that this umpolung reaction proceeds through the generation of a Ru-nitrenoid followed by concerted [4 + 2] cycloaddition with CO(2). |
format | Online Article Text |
id | pubmed-5982211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-59822112018-06-15 Ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2) Yan, Si-Shun Zhu, Lei Ye, Jian-Heng Zhang, Zhen Huang, He Zeng, Huiying Li, Chao-Jun Lan, Yu Yu, Da-Gang Chem Sci Chemistry The first ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2) to generate important aryl acetic acids is reported. Besides aldehyde hydrazones, a variety of ketone hydrazones, which have not been successfully applied in previous umpolung reactions with other reactive electrophiles, also show high reactivity and selectivity under mild conditions. Moreover, this operationally simple protocol features good functional group tolerance, is readily scalable, and offers easy derivation of important structures, including bioactive felbinac and adiphenine. Computational studies reveal that this umpolung reaction proceeds through the generation of a Ru-nitrenoid followed by concerted [4 + 2] cycloaddition with CO(2). Royal Society of Chemistry 2018-04-30 /pmc/articles/PMC5982211/ /pubmed/29910940 http://dx.doi.org/10.1039/c8sc01299g Text en This journal is © The Royal Society of Chemistry 2018 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Yan, Si-Shun Zhu, Lei Ye, Jian-Heng Zhang, Zhen Huang, He Zeng, Huiying Li, Chao-Jun Lan, Yu Yu, Da-Gang Ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2) |
title | Ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2)
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title_full | Ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2)
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title_fullStr | Ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2)
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title_full_unstemmed | Ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2)
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title_short | Ruthenium-catalyzed umpolung carboxylation of hydrazones with CO(2)
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title_sort | ruthenium-catalyzed umpolung carboxylation of hydrazones with co(2) |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5982211/ https://www.ncbi.nlm.nih.gov/pubmed/29910940 http://dx.doi.org/10.1039/c8sc01299g |
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