<b>The Chemistry of Carbonyl Fluoride. I. The Fluorination of Organic Compounds</b>
作者:F. S. Fawcett、C. W. Tullock、D. D. Coffman
DOI:10.1021/ja00881a017
日期:1962.11
Carbonylfluoride is a versatile intermediate to organic fluorine compounds. Its reaction with carbonyl compounds such as cyclohexanone, benzaldehyde and benzophenone gives the gem-difluorides, while N,N-dimethylformamide yields a,a-difluorotrimethylamine. Metal fluoride-catalyzed addition at the ethylenic bond in perfluoroolefins forms perfluoroacyl fluorides, while the C--?! unsaturated compounds
The Electrochemical Fluorination of Aliphatic Primary Monohydric Alcohols and Aldehydes
作者:Takashi Abe、Shunji Nagase、Hajime Baba
DOI:10.1246/bcsj.49.1888
日期:1976.7
fluorides were obtained by the electrochemical fluorination of primary monohydricalcohols and aldehydes containing 4–8 carbon atoms. The five-membered rather than the six-membered perfluorocyclic ethers were formed as the cyclic products. The over-all yields of the perfluorocyclic ethers and the perfluoroalkanoyl fluorides from the alcohols were in the range of 10–20%, and 3–12% respectively. Those from