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Chemical Structure| 288-99-3 Chemical Structure| 288-99-3
Chemical Structure| 288-99-3

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David F. León Rayo ; Laurie-Anne Jouanno ; Fabien Gagosz ;

Abstract: Among the different methods allowing the introduction of a CF3 group into an organic framework, those based on the use of a fluorinated carbene intermediate are particularly useful. They can lead to the formation of structural motifs that are difficult to access by other means. We report in this article the development of a new route allowing the generation of an α-trifluoromethyl α-benzyloxy carbene from a readily accessible trifluoromethyl 1,3,4-oxadiazoline. Trapping of the carbene in the presence of various alkynes led to the formation of various protected trifluoromethyl tertiary cyclopropenols in moderate yields.

Keywords: (trifluoromethyl)carbene ; oxadiazoline ; cyclopropene

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Product Details of 1,3,4-Oxadiazole

CAS No. :288-99-3
Formula : C2H2N2O
M.W : 70.05
SMILES Code : O1C=NN=C1
MDL No. :MFCD00955535
InChI Key :FKASFBLJDCHBNZ-UHFFFAOYSA-N
Pubchem ID :97428

Safety of 1,3,4-Oxadiazole

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 1,3,4-Oxadiazole

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 288-99-3 ]
 

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