3-Aryl-2,4-pentanediones from 3,5-dimethyl-4-iodoisoxazoles: An application of a palladium-catalyzed cross-coupling reaction

Article abstract of DOI:10.1080/00397919408012650

3,5-Dimethyl-4-iodoisoxazole readily undergoes palladium-catalyzed coupling with arylboronic acids and organostannanes to form 4-aryl-3,5- dimethylisoxazoles. The unique nature of the isoxazole-ring is exploited to convert 4-aryl-3,5-dimethylisoxazoles to

Full text of DOI:10.1080/00397919408012650

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Synthetic Communications: An
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3-Aryl-2,4-pentanediones from
3,5-Dimethyl-4-iodoisoxazoles:
An Application of a Palladium-
Catalyzed Cross-Coupling
Reaction
Sharada S. Labadie a
a Institute of Organic Chemistry Syntex Discovery
Research , Palo Alto, California, 94304
Published online: 23 Sep 2006.
To cite this article: Sharada S. Labadie (1994) 3-Aryl-2,4-pentanediones from
3,5-Dimethyl-4-iodoisoxazoles: An Application of a Palladium-Catalyzed Cross-
Coupling Reaction, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 24:5, 709-719, DOI:
10.1080/00397919408012650
To link to this article: http://dx.doi.org/10.1080/00397919408012650
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