SEARCH Articles Figures Tables A4-Oxocene, 2,8-disubstituted via cyclization of oxonium ions Alcohols oxonium ion formation Alkyl-aluminumsilyl oxonium ions Alkyl-aluminumsilyl oxonium ions formation Alkyl-aluminumsilyl oxonium ions theoretical calculations Alkyl-aluminumsilyl oxonium ions zeolite Blue oxonium ions Carbenium-oxonium ion equilibria Carbocations on surfaces aluminumsilyl oxonium ion Carbocations oxonium ions Carotenoid oxonium ions Crown ethers oxonium ion binding Hydride transfer to cyclic oxonium ion Metals Oxonium ions Oxonium Oxonium and ammonium ion-exchange Oxonium ion crown ether complexes Oxonium ion equilibria Oxonium ion intermediate Oxonium ion pair Oxonium ion salts Oxonium ions acidity Oxonium ions arenes Oxonium ions bicyclo Oxonium ions chiral Oxonium ions cleavage Oxonium ions formation Oxonium ions halides Oxonium ions initiators Oxonium ions long-lived Oxonium ions phenols Oxonium ions polyene cyclization Oxonium ions primary Oxonium ions reaction Oxonium ions reaction with enol silanes Oxonium ions reduction Oxonium ions secondary Oxonium ions silicon-stabilized Oxonium ions superelectrophiles Oxonium ions superelectrophilic Oxonium ions tertiary Oxonium ions trifluoromethyl Oxonium ions, mass spectra Oxonium ions, nucleophilic attack Oxonium ions, ring opening Oxonium ions, secondary equilibria Oxonium ions, secondary preparation Oxonium ions, secondary stability Oxonium ions, secondary structure Oxonium ions, secondary tertiary Oxonium ions, stereoselective Oxonium ions, stereoselective glycosylations with Transition state oxonium ion dissociation