期刊
JOURNAL OF FLUORINE CHEMISTRY
卷 169, 期 -, 页码 38-49出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jfluchem.2014.11.001
关键词
Functionalization of gem difluoromethyl; group Carbon-carbon bond formation; Base promoted addition reaction
资金
- Department of Science and Technology, New Delhi
From gem-difluoromethyl group of 1,1,2,2-tetrafluoroethyl ether and 2,2-difluoroalkylamide, proton can be removed by potassium bis(trimethylsilyl)amide in DMF, THF or toluene. The generated nucleophiles are then condensed with benzophenones, benzaldehydes or Schiffs bases to provide new fluorinated alcohols and amines. Some interesting solvent effects are also observed., (C) 2014 Elsevier B.V. All rights reserved.
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