Staudinger Azide Reduction: Synthesis of Amine
Staudinger reaction is an organic name reaction of organic azides with trivalent phosphorous compounds (e.g., trialkyl- or triarylphosphines) to afford the corresponding aza-ylides.
amine synthesis
Sommelet-Hauser Rearrangement
Sommelet-Hauser rearrangement is one of the thermal [2,3]-sigmatropic rearrangements, in which the benzylic quaternary ammonium salts are treated within the presence of a strong base like NaNH2, KNH2, as well as alkyl lithium to prepare the Substituted 3° benzylic amine.