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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...

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Autores principales: Kato, Hiroki, Musha, Itsuki, Komatsuda, Masaaki, Muto, Kei, Yamaguchi, Junichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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