SEARCH Articles Figures Tables 1.5- Naphthyridine, amino-, formation nucleophilic substitution Alcohols as Nucleophiles and Electrophiles Formation of Tosylates Carbon-oxygen single bond formation oxygenated nucleophiles Double bond formation nitrogen nucleophiles Double bond formation nucleophilic trapping Double bond formation oxygen nucleophiles Formates hydrolysis, nucleophile Hydrolysis formates, nucleophile isotope Imine formation nucleophilic alkyl substitution Imine formation nucleophilic aromatic substitution Nitrogen nucleophiles formation Nucleophile isotope effects formate hydrolysis Nucleophiles amine formation Nucleophiles carbon-phosphorus bond formation Nucleophilic Addition of Alcohols Acetal Formation Nucleophilic Addition of Amines Imine and Enamine Formation Nucleophilic Addition of Grignard and Hydride Reagents Alcohol Formation Nucleophilic Addition of HCN Cyanohydrin Formation Nucleophilic carbenes bond formations Nucleophilic constant formation Nucleophilic cyclization ring-formation Nucleophilic groups formation Nucleophilic substitution diene selective formation Nucleophilic substitution formate reactions Nucleophilic substitution formation Nucleophilic substitution reactions amine formation Nucleophilic substitutions 1,3,5-triazines formation Nucleophilic substitutions ether formation Oxygen nucleophiles formation Pyridinium cation, formation nucleophilic reactions Soft carbon nucleophiles formation Sulfur nucleophiles formation Triple bond formation nitrogen nucleophiles Triple bond formation oxygen nucleophiles