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Catalytic three-component C–C bond forming dearomatization of bromoarenes with malonates and diazo compounds
A Pd-catalyzed dearomative three-component C–C bond formation of bromoarenes with diazo compounds and malonates was developed. Various bromoarenes ranging from benzenoids to azines and heteroles were transformed to the corresponding substituted alicyclic molecules. The key to this reaction is the ge...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163412/ https://www.ncbi.nlm.nih.gov/pubmed/34123130 http://dx.doi.org/10.1039/d0sc02881a |
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author | Kato, Hiroki Musha, Itsuki Komatsuda, Masaaki Muto, Kei Yamaguchi, Junichiro |
author_facet | Kato, Hiroki Musha, Itsuki Komatsuda, Masaaki Muto, Kei Yamaguchi, Junichiro |
author_sort | Kato, Hiroki |
collection | PubMed |
description | A Pd-catalyzed dearomative three-component C–C bond formation of bromoarenes with diazo compounds and malonates was developed. Various bromoarenes ranging from benzenoids to azines and heteroles were transformed to the corresponding substituted alicyclic molecules. The key to this reaction is the generation of a benzyl–palladium intermediate, which reacts with malonates to form a Pd–O-enolate species. Strikingly, the present method enabled rapid access to multi-substituted alicycles through subsequent elaboration of dearomatized products. |
format | Online Article Text |
id | pubmed-8163412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81634122021-06-11 Catalytic three-component C–C bond forming dearomatization of bromoarenes with malonates and diazo compounds Kato, Hiroki Musha, Itsuki Komatsuda, Masaaki Muto, Kei Yamaguchi, Junichiro Chem Sci Chemistry A Pd-catalyzed dearomative three-component C–C bond formation of bromoarenes with diazo compounds and malonates was developed. Various bromoarenes ranging from benzenoids to azines and heteroles were transformed to the corresponding substituted alicyclic molecules. The key to this reaction is the generation of a benzyl–palladium intermediate, which reacts with malonates to form a Pd–O-enolate species. Strikingly, the present method enabled rapid access to multi-substituted alicycles through subsequent elaboration of dearomatized products. The Royal Society of Chemistry 2020-07-29 /pmc/articles/PMC8163412/ /pubmed/34123130 http://dx.doi.org/10.1039/d0sc02881a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Kato, Hiroki Musha, Itsuki Komatsuda, Masaaki Muto, Kei Yamaguchi, Junichiro Catalytic three-component C–C bond forming dearomatization of bromoarenes with malonates and diazo compounds |
title | Catalytic three-component C–C bond forming dearomatization of bromoarenes with malonates and diazo compounds |
title_full | Catalytic three-component C–C bond forming dearomatization of bromoarenes with malonates and diazo compounds |
title_fullStr | Catalytic three-component C–C bond forming dearomatization of bromoarenes with malonates and diazo compounds |
title_full_unstemmed | Catalytic three-component C–C bond forming dearomatization of bromoarenes with malonates and diazo compounds |
title_short | Catalytic three-component C–C bond forming dearomatization of bromoarenes with malonates and diazo compounds |
title_sort | catalytic three-component c–c bond forming dearomatization of bromoarenes with malonates and diazo compounds |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8163412/ https://www.ncbi.nlm.nih.gov/pubmed/34123130 http://dx.doi.org/10.1039/d0sc02881a |
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