Synthesis of spiroisoindolinones by palladium-catalyzed heterocyclization of 2-iodobenzoyl chloride with ketimines
โ Scribed by Chan Sik Cho; Xue Wu; Li Hong Jiang; Sang Chul Shim; Hong Rak Kim
- Book ID
- 102340395
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1999
- Tongue
- English
- Weight
- 263 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-152X
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โฆ Synopsis
2-Iodobenzoyl chloride reacts with ketimines in acetonitrile at (100^{\circ}) under carbon monoxide pressure in the presence of a catalytic amount of a palladium catalyst together with triethylamine to afford the corresponding spiroisoindolinones in high yields.
๐ SIMILAR VOLUMES
Imidoyl chlorides were successfully transformed into ketimines when treated with organotin compounds in the presence of palladium complex catalysts. Reduction and alkylation of imidoyl chlorides into imines are important reactions of practical potential for the synthesis of B-lactam antibiotics. 132
2-Iodobenzoyl chloride reacts with an array of imines in acetonitrile-methanol under carbon monoxide pressure in the presence of a catalytic amount of bis(triphenylphosphine)palladium(II) chloride/triphenylphosphine together with triethylamine to afford the corresponding isoindolin-1-ones in moderat
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