Synthesis of Functionalized Azepines via Cu(I)-Catalyzed Tandem Amination/Cyclization Reaction of Fluorinated Allenynes

An efficient method for the selective preparation of trifluoromethyl-substituted azepin-2-carboxylates and their phosphorous analogues has been developed via Cu(I)-catalyzed tandem amination/cyclization reaction of functionalized allenynes with primary and secondary amines.

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2022-08, Vol.27 (16), p.5195
Hauptverfasser: Philippova, Anna N, Vorobyeva, Daria V, Gribanov, Pavel S, Godovikov, Ivan A, Osipov, Sergey N
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Sprache:eng
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Zusammenfassung:An efficient method for the selective preparation of trifluoromethyl-substituted azepin-2-carboxylates and their phosphorous analogues has been developed via Cu(I)-catalyzed tandem amination/cyclization reaction of functionalized allenynes with primary and secondary amines.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules27165195