SEARCH Articles Figures Tables A variety of electrophilic alkenes will accept enol(ate) nucleophiles Alkene complexes nucleophilic addition Alkene complexes nucleophilic attack Alkene derivatives carbon nucleophile reactions Alkene derivatives nucleophilic substitution, heteroatomic Alkene ligands nucleophilic attack Alkene nucleophilicity Alkene radical cations, kinetics nucleophiles, reaction with Alkenes as nucleophile Alkenes as nucleophiles Alkenes as nucleophiles or electrophiles Alkenes asymmetric nucleophilic addition Alkenes carbon nucleophiles Alkenes coordinated, nucleophilic attack Alkenes nitrogen nucleophiles Alkenes nucleophilic addition Alkenes nucleophilic additions, carbanion intermediates Alkenes nucleophilic attack Alkenes nucleophilic capture Alkenes nucleophilic substitution Alkenes nucleophilic, basicity Alkenes oxygen nucleophiles Alkenes polarizable nucleophiles Alkenes relative nucleophilicity Alkenes soft nucleophile Alkenes, Alkynes, Enols, and Vinyl Amines as the Nucleophiles Cyclofunctionalization of Alkynes and Alkenes Bearing Pendant Nucleophiles External attack of nucleophiles on alkene coordinated to electrophilic metal complexes Fluorinated alkenes reactions with nucleophiles Group 16 atoms, nucleophilic substitution alkene-alcohol reactions Heteroatomic nucleophiles alkene precursors Mercury-Mediated Nucleophilic Addition to Alkenes Nucleophiles alkene complexes Nucleophiles alkene, formaldehyde Nucleophilic Addition to Alkenes and Alkynes Nucleophilic conjugate addition to alkenes Nucleophilic reactions alkenes Orbital Interaction Between a Nucleophilic Radical and an Electron-poor Alkene Oxygen nucleophiles alkenes alkynes allenes Palladium -catalyzed nucleophilic additions, alkenes Reactions with Alkene Nucleophiles Ring-Opening Unsymmetrical Oxa- and Aza-bicyclic Alkenes with Heteroatom Nucleophiles Ring-Opening meso-Oxabicyclic Alkenes with Nitrogen-Based Nucleophiles