Mannich reaction of trifluoroacetaldehyde hydrazones, a useful entry to trifluoromethyl substituted heterocycles. - École polytechnique
Article Dans Une Revue Organic & Biomolecular Chemistry Année : 2018

Mannich reaction of trifluoroacetaldehyde hydrazones, a useful entry to trifluoromethyl substituted heterocycles.

Résumé

NH-aryl hydrazones derived from trifluoroacetaldehyde hemiacetal may be involved in efficient Mannich type reactions with formaldehydes and aromatic aldehydes. The resulting hydrazones are useful building blocks for the preparation of trifluoromethyl substituted heterocycles as shown by a straightforward preparation of 1,2-diazine derivatives under heating with β-ketoesters.

Domaines

Chimie organique
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Dates et versions

hal-02095052 , version 1 (14-01-2024)

Licence

Copyright (Tous droits réservés)

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Citer

Shuanglong Jia, Laurent El Kaim. Mannich reaction of trifluoroacetaldehyde hydrazones, a useful entry to trifluoromethyl substituted heterocycles.. Organic & Biomolecular Chemistry, 2018, 16 (9), pp.1457-1460. ⟨10.1039/c7ob02840g⟩. ⟨hal-02095052⟩
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