Strecker Reaction :Synthesis of Amino Acids| Mechanism
The most well-known use of the Strecker reaction, α-amino nitriles, is their hydrolysis under acidic or basic conditions to obtain α-amino acids (Strecker amino acid synthesis).
Name Reaction
Perkin Reaction (Perkin Condensation): definition| mechanism| example| application
The Perkin reaction (or Perkin condensation) is an condensation of aromatic aldehydes and the anhydrides of aliphatic carboxylic acids in the presence of a weak base to obtain α,β-unsaturated carboxylic acids
Staudinger Ketene Cycloaddition: Definition |Mechanism
here, we defined Staudinger Ketene Cycloaddition, includes Definition, Mechanism, staudinger cycloaddition |cycloaddition of ketene
Simmons-Smith Reaction Mechanism
Simmon Smith reaction is most powerful organic cheletropic (reaction) method for cyclopropane preparation from diiodomethane (CH2I2) in the presence of zinc-copper couple (Zn-Cu) from unfunctionalized alkenes (e.g., cyclohexene, styrene) stereospecifically.