期刊
CHINESE JOURNAL OF CHEMISTRY
卷 35, 期 11, 页码 1673-1677出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cjoc.201700191
关键词
Beckmann rearrangement; oganocatalyst; ketoximes; amides
资金
- Shaanxi Provincial Key Laboratory Project [15JS004]
- Baoji University of Arts and Sciences [ZK15046]
An efficient Beckmann rearrangement of ketoximes was developed using carbon tetrabromide/ triphenylphosphine as an organocatalyst without addition of any acids or metals. The reaction showed good functional group tolerance and gave various amides in moderate to good yields.
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