Epoxidation is treatment where an electrophilic oxidizing agent is capable of introducing a single oxygen atom to...
Buchler Glossary
Alkynylation is an addition reaction in organic synthesis where a terminal alkyne adds to a carbonyl group to form an α-alkynyl alcohol. When the acetylide is formed from acetylene, the reaction gives an α-ethynyl alcohol. This process is often referred to as ethynylation.
Please find several examples of Alkynylation reactions promoted by Cinchona Alkaloids in our Buchler Chiral Catalyst Search.
Example from literature
Practical Asymmetric Conjugate Alkynylation of Meldrum’s Acid-Derived Acceptors: Access to Chiral β-Alkynyl Acids. (Cui et al.; J. Am. Chem. Soc. 2010, 132, 2, 436-437.)
Further Articles:
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Fluorination is for instance a replacement of one hydrogen atom within a molecule by fluorine. The incorporation of...
Asymmetric Friedel-Crafts
Friedel-Crafts reactions in organic chemistry are referred to two main types of reactions, known as alkylation...
Asymmetric Henry Reaction (Nitroaldol Reaction)
The Henry reaction, also called Nitroaldol reaction, is a classic carbon–carbon bond formation reaction in organic...
Asymmetric Hydrogenation
Hydrogenation is a reduction reaction which results in an addition of hydrogen (often as H2). If an organic compound...
Asymmetric Mannich Reaction
In general the Mannich reaction is an aminoalkylation reaction, involving the condensation of an enolizable carbonyl...