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...
Clemmensen Reduction

Clemmensen Reduction

The Clemmensen reduction allows the conversion of a carbonyl group to the corresponding methylene group using zinc amalgam and concentrated hydrochloric acid. Due to its original harsh conditions, the Clemmensen reduction is rarely used in modern organic synthesis....

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