4.6 Article

Conversion between Difluorocarbene and Difluoromethylene Ylide

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 19, 期 45, 页码 15261-15266

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201303248

关键词

carbenes; difluorocyclopropanation; difluoro-olefination; fluorine; ylides

资金

  1. National Natural Science Foundation [21032006, 21172240]
  2. 973 Program of China [2012CBA01200]
  3. Chinese Academy of Sciences

向作者/读者索取更多资源

The interconversion between difluoromethylene ylide and difluorocarbene is described. The difluoromethylene ylide precursor, Ph3P+CF2CO2-, could be turned into an efficient difluorocarbene reagent, whereas the classical difluorocarbene reagents, HCF2Cl and FSO2CF2CO2TMS, could generate highly reactive difluoromethylene ylide. Thus the Wittig difluoro-olefination and difluorocyclopropanation could be selectively realized by using the same reagent. In addition, the ylides obtained from different carbene sources showed different reactivity in Wittig reactions.

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