A transition-metal-free fast track to flavones and 3-arylcoumarins
A highly regioselective and transition-metal free one-pot arylation of chromenones with arylboronic acids has been achieved employing K2S2O8. The procedure consists of a sequence of some reactions including an arylation/decarboxylation cascade and proceeds well in aqueous media to afford biologically interesting flavones and 3-arylcoumarins. This method exhibited excellent selectivity and functional group tolerance under mild conditions. The reaction also showed perfect efficacy for the preparation of styryl coumarins.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2017 |
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Erschienen: |
2017 |
Enthalten in: |
Zur Gesamtaufnahme - volume:53 |
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Enthalten in: |
Chemical communications (Cambridge, England) - 53(2017), 77 vom: 26. Sept., Seite 10676-10679 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Golshani, Mostafa [VerfasserIn] |
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Links: |
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Themen: |
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Anmerkungen: |
Date Completed 05.03.2018 Date Revised 05.03.2018 published: Print Citation Status PubMed-not-MEDLINE |
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doi: |
10.1039/c7cc02107k |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM275758486 |
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520 | |a A highly regioselective and transition-metal free one-pot arylation of chromenones with arylboronic acids has been achieved employing K2S2O8. The procedure consists of a sequence of some reactions including an arylation/decarboxylation cascade and proceeds well in aqueous media to afford biologically interesting flavones and 3-arylcoumarins. This method exhibited excellent selectivity and functional group tolerance under mild conditions. The reaction also showed perfect efficacy for the preparation of styryl coumarins | ||
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