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Novel and efficient one-step parallel synthesis of dibenzopyranones via Suzuki-Miyaura cross coupling.


ABSTRACT: Microwave-promoted novel and efficient one-step parallel synthesis of dibenzopyranones and heterocyclic analogues from bromo arylcarboxylates and o-hydroxyarylboronic acids via Suzuki-Miyaura cross coupling reaction is described. Spontaneous lactonization gave dibenzopyranones and heterocyclic analogues bearing electron-donating and -withdrawing groups on both aromatic rings in good to excellent yields.

SUBMITTER: Vishnumurthy K 

PROVIDER: S-EPMC3921962 | biostudies-literature | 2010 Sep

REPOSITORIES: biostudies-literature

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Novel and efficient one-step parallel synthesis of dibenzopyranones via Suzuki-Miyaura cross coupling.

Vishnumurthy Kodumuru K   Makriyannis Alexandros A  

Journal of combinatorial chemistry 20100901 5


Microwave-promoted novel and efficient one-step parallel synthesis of dibenzopyranones and heterocyclic analogues from bromo arylcarboxylates and o-hydroxyarylboronic acids via Suzuki-Miyaura cross coupling reaction is described. Spontaneous lactonization gave dibenzopyranones and heterocyclic analogues bearing electron-donating and -withdrawing groups on both aromatic rings in good to excellent yields. ...[more]

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