Abstract
2-Iodobenzoyl chloride reacts with aldimines in acetonitrile at 100° under carbon monoxide in the presence of a catalytic amount of bis(triphenylphosphine)palladium(II) chloride together with triethylamine to give the corresponding 3-alkenylisoindolin-1-ones in good yields.
| Original language | English |
|---|---|
| Pages (from-to) | 265-268 |
| Number of pages | 4 |
| Journal | Journal of Heterocyclic Chemistry |
| Volume | 35 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1998 |
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Dive into the research topics of 'Synthesis of 3-Alkenylisoindolin-1-ones via Palladium(0)-Catalyzed Coupling and Cyclization between 2-Iodobenzoyl Chloride and Aldimines'. Together they form a unique fingerprint.Cite this
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