N-benzyl-N,N,N-triethylammonium chloride; pentacarbonyliron(0) in sodium hydroxide P=760 Torr; 12 h; Ambient temperature;

N-benzyl-N,N,N-triethylammonium chloride; pentacarbonyliron(0) in hexane P=760 Torr; 48 h; Ambient temperature; Yield given;

N-benzyl-N,N,N-triethylammonium chloride; pentacarbonyliron(0) in sodium hydroxide; toluene P=760 Torr; 48 h; Ambient temperatureother temperature, other reaction times, other or without solvents;

sodium hydroxide; [(1,5-cyclooctadiene)Rh(triphenylphosphine)2]PF6; tetra-n-hexylammonium hydrogen sulfate in dichloromethane T=40°C; P=760 Torr;

sodium hydroxide; η6-C6H6BPh3-Rh(COD)+; tetra-n-hexylammonium hydrogen sulfate in dichloromethane T=40°C; P=760 Torr; other substituted benzylic and allylic bromides; var. phase transfer catalysts; var. rhodium catalysts; MechanismProduct distribution;

diethyl ether; ammonia; KNH2 anschliessend Behandeln mit Benzylchlorid;