Alkynylation

Alkynylation

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  Acetylide carbonyl addition

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  Arens-van Dorp Reaction Isler Modification

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  Reppe chemistry endiol

Alkynylation

Alkynylation is a chemical reaction that involves the introduction of an alkyne moiety into a molecule. This process is a valuable tool in organic chemistry for the synthesis of complex molecules, as alkynes are versatile intermediates that can undergo a variety of transformations.

Mechanism

The mechanism of alkynylation typically involves the formation of a carbon-carbon bond between an alkyne and another organic substrate. This can be achieved through several methods, including:

• Nucleophilic Alkynylation: This involves the use of a nucleophilic alkyne, such as a lithium acetylide or a Grignard reagent, to attack an electrophilic center, such as a carbonyl group or an alkyl halide.

• Transition Metal-Catalyzed Alkynylation: Transition metals such as palladium, copper, and nickel can catalyze the coupling of alkynes with various electrophiles. The Sonogashira coupling is a well-known example, where a terminal alkyne is coupled with an aryl or vinyl halide in the presence of a palladium catalyst and a copper co-catalyst.

Applications

Alkynylation reactions are widely used in the synthesis of natural products, pharmaceuticals, and materials science. The introduction of an alkyne group can provide a handle for further functionalization, such as:

• Cycloaddition Reactions: Alkynes can participate in cycloaddition reactions, such as the Diels-Alder reaction and the Huisgen cycloaddition, to form cyclic structures.

• Hydrogenation: Alkynes can be selectively hydrogenated to form alkenes or alkanes, allowing for the controlled reduction of the alkyne moiety.

• Click Chemistry: The copper-catalyzed azide-alkyne cycloaddition (CuAAC) is a popular "click chemistry" reaction that forms 1,2,3-triazoles, which are useful in drug discovery and bioconjugation.

Related Pages

• Alkyne
• Sonogashira coupling
• Cycloaddition
• Click chemistry
• Transition metal catalysis