SEARCH Articles Figures Tables 1.3- Oxazin-2-one N-acyliminium ions A -Acyliminium cyclizations A-Acyliminium ion cyclization A-Acyliminium ion cyclization intramolecular A-Acyliminium ions generation A-Acyliminium ions reactions A-Acyliminium salts A-acyliminium ions Acetals V-acyliminium ion reactions Acylimine/acyliminium precursors Acyliminium cations Acyliminium cyclization Acyliminium ion cyclization Acyliminium ion, formation Acyliminium ions Bisamides V-acyliminium ion precursors Bisureas V-acyliminium ion precursors Cyclization Pictet-Spengler acyliminium Cyclization acyliminium-mediated Elaeokanines via acyliminium ion terminated cyclization Erythrinan acyliminium ions Gelsemine V-acyliminium ions Glycine, cyclopentylsynthesis N-acyliminium ions IV-Acyliminium ions Iminium acyliminium Isoquinoline, perhydrosynthesis V-acyliminium ions JV-Acyliminium ions Lewis-acid-catalyzed Nucleophilic Addition of Functionalized Alkenyl Boronic Esters to Activated N-acyliminium Ions Mesembrine V-acyliminium ions N-Acyliminium N-Acyliminium ions N-Acyliminium salts N-acyliminium ion cyclizations N-acyliminium ion reaction N-acyliminium ions generation OVERMAN D. J. RICCA, University of California, Irvine, CA, USA 5 Additions to V-Acyliminium Ions Pyrrolidines V-acyliminium ions Pyrrolidinone, 5-acetoxyV-acyliminium ion intermediate Pyrrolizidines V-acyliminium ions Rearrangement acyliminium ions Stannane, allenylreaction with N-acyliminium ions Stannane, allenylreaction with N-acyliminium ions synthesis Stiles’ reagent V-acyliminium ions TV-Acyliminium ions TV-Acyliminium ions dissociation V-Acyliminium V-Acyliminium ions V-Acyliminium ions Diels-Alder dienophiles V-Acyliminium ions addition reactions V-Acyliminium ions as Diels-Alder dienes V-Acyliminium ions as carbocations V-Acyliminium ions electrophilicity V-Acyliminium ions generation V-Acyliminium ions intermolecular reactions V-Acyliminium ions intramolecular reactions V-Acyliminium ions reactions V-Acyliminium ions reviews