Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 6, Pages 2052-+Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja8084065
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Funding
- MEXT, Japan
- JSPS
- Eisai and Kyoto University
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A novel synthetic method for the preparation of tri- or tetrasubstituted epoxides is reported. Treatment of readily available tertiary allyl alcohol with aryl or alkenyl, halide under palladium catalysis resulted in arylative cyclization to form the epoxide. The reaction includes intramotecular C-O bond and intermolecular C-C bond construction.
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