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2000
Volume 24, Issue 18
  • ISSN: 1385-2728
  • E-ISSN: 1875-5348

Abstract

The development of an efficient and mild synthetic methodology for the construction of bioactive fluorine-containing molecules represents one of the hot research topics in general synthetic organic chemistry. In this review, some recent progresses achieved in the development of detrifluoroacetylatively generated mono-fluorinated enolates via CC bond cleavage and their asymmetric nucleophilic reactions for assembly of chiral quaternary C-F center containing compounds.

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/content/journals/coc/10.2174/1385272824999200801022712
2020-09-01
2025-05-26
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/content/journals/coc/10.2174/1385272824999200801022712
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