期刊
CHEMISTRY LETTERS
卷 34, 期 12, 页码 1688-1689出版社
CHEMICAL SOC JAPAN
DOI: 10.1246/cl.2005.1688
关键词
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FeCl3-promoted regioselective ring-opening reactions of cyc lopropyl trimethylsilyl ethers, obtained by SMI2 reduction c followed by silylation with Me3SiCl of bromoalkyl ketones and acyl chloride, were performed. Eventually, the sequential reduction and oxidation reactions starting from bromoalkyl ketones to give ring-expanded enones were achieved in one-pot.
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