期刊
CHINESE JOURNAL OF ORGANIC CHEMISTRY
卷 38, 期 6, 页码 1469-1476出版社
SCIENCE PRESS
DOI: 10.6023/cjoc201712036
关键词
trifluoromethyl building blocks; cycloaddition; trifluoromethylated N-acylhydrazones; alkenes; trifluoromethyl pyrazolidines; trifluoromethyl pyrazolines
资金
- National Natural Science Foundation of China [21662030, 21462037]
A Lewis acid-catalyzed [3+2] cycloaddition of trifluoromethylated N-acylhydrazones with alkenes was explored, and a series of CF3-substituted pryazolidines were obtained in high yields (up to 91%). The reaction features the use of cheap and readily available trifluoromethylated N-acylhydrazones as trifluoromethyl building blocks, mild reaction conditions and easy operation. Furthermore, the cycloadducts can be transformed into trifluoromethylated pyrazolines in excellent yields.
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