Aryltrifluoromethylsulfoxides: Sulfinylation or Aromatics by Triflinate Salts in Acid Medium - Archive ouverte HAL
Article Dans Une Revue SYNLETT Année : 2001

Aryltrifluoromethylsulfoxides: Sulfinylation or Aromatics by Triflinate Salts in Acid Medium

Résumé

Direct sulfinylation reaction of simple aromatic compounds by triflinate salts in triflic acid led to aryltrifluoromethyl sulfoxides. The para isomer was the major one. The regioselectivity of the reaction was very high when the substituent on the aromatic ring was a halogen atom, a trifluoromethoxy group or an acetanilide function.

Domaines

Chimie organique
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Dates et versions

hal-00095229 , version 1 (15-09-2006)

Identifiants

Citer

Marc Tordeux, Claude Wakselman, Céline Freslon, Laurent Saint-Jalmes. Aryltrifluoromethylsulfoxides: Sulfinylation or Aromatics by Triflinate Salts in Acid Medium. SYNLETT, 2001, 0, pp.550. ⟨10.1055/s-2001-12316⟩. ⟨hal-00095229⟩

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