Baeyer-Villiger oxidation

The Baeyer-Villiger oxidation allows the transformation of ketones into esters and cyclic ketones into lactones by the use of a wide range of peroxyacids, being m-CPBA the most common. The regiochemistry depends on the migratory capacity of the alkyl groups, with the...
Suzuki Coupling

Suzuki Coupling

The Suzuki coupling, or Suzuki–Miyaura reaction, is a palladium-catalyzed cross-coupling between organoboronic acids or esters and organic halides or triflates under basic conditions to form a new C–C sigma bond. The Suzuki coupling reaction is performed between an...
Buchwald-Hartwig Coupling

Buchwald-Hartwig Coupling

The Buchwald-Hartwig coupling is a direct Pd-catalyzed C–N or C–O bond formation reaction between aryl halides and amines or alcohols, typically conducted in the presence of a stoichiometric amount of base. The coupling can be both intermolecular and intramolecular...
Michael Reaction

Michael Reaction

The Michael reaction or Michael addition is a C–C bond-forming reaction. It consists of the nucleophilic addition of an activated nucleophile (Michael donor) to an α,β-unsaturated carbonyl compound (Michael acceptor). It belongs to the class of conjugate additions or...
Wolff-Kishner Reduction

Wolff-Kishner Reduction

The Wolff-Kishner reduction allows the deoxygenation of aldehydes and ketones to hydrocarbons via the corresponding hydrazones under basic conditions and heat. The reaction is commonly employed to remove a carbonyl group after it has served its synthetic purpose in...
Reimer-Tiemann Reaction

Reimer-Tiemann Reaction

The Reimer-Tiemann reaction facilitates the formylation of phenols using chloroform and a strong base, typically an aqueous hydroxide solution. The reaction proceeds via electrophilic aromatic substitution with the formed dichlorocarbene. While the regioselectivity is...