4.8 Article

Palladium-Catalyzed Carbonylation-Decarboxylation of Diethyl(2-iodoaryl)malonates with Imidoyl Chlorides: An Efficient Route to Substituted Isoquinolin-1(2H)-ones

Journal

ORGANIC LETTERS
Volume 10, Issue 21, Pages 4903-4906

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol801991m

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Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)

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A wide variety of substituted isoquinolin-1(2H)-ones were synthesized in reasonable to good yields by the palladium-catalyzed cyclization of diethyl(2-iodoaryl)malonates with imidoyl chlorides and carbon monoxide in tetrahydrofuran. A palladium-catalyzed carbonylation-decarboxylation process may be involved in the one-step synthesis of the isoquinolin-1(2H)-ones.

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