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11 relations: Aldehyde, Aldol reaction, Cascade reaction, Diastereomer, Enol, Hydrolysis, Hydroxy group, Ketone, Lithium diisopropylamide, Organic synthesis, Tishchenko reaction.
Aldehyde
An aldehyde or alkanal is an organic compound containing a functional group with the structure −CHO, consisting of a carbonyl center (a carbon double-bonded to oxygen) with the carbon atom also bonded to hydrogen and to an R group, which is any generic alkyl or side chain.
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Aldol reaction
The aldol reaction is a means of forming carbon–carbon bonds in organic chemistry.
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Cascade reaction
A cascade reaction, also known as a domino reaction or tandem reaction, is a chemical process that comprises at least two consecutive reactions such that each subsequent reaction occurs only in virtue of the chemical functionality formed in the previous step.
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Diastereomer
Diastereomers (sometimes called diastereoisomers) are a type of a stereoisomer.
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Enol
Enols, or more formally, alkenols, are a type of reactive structure or intermediate in organic chemistry that is represented as an alkene (olefin) with a hydroxyl group attached to one end of the alkene double bond.
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Hydrolysis
Hydrolysis is a term used for both an electro-chemical process and a biological one.
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Hydroxy group
A hydroxy or hydroxyl group is the entity with the formula OH.
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Ketone
In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.
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Lithium diisopropylamide
Lithium diisopropylamide (commonly abbreviated LDA) is a chemical compound with the molecular formula 2NLi.
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Organic synthesis
Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds.
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Tishchenko reaction
The Tishchenko reaction is an organic chemical reaction that involves disproportionation of an aldehyde in the presence of an alkoxide.
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Aldol-Tishchenko reaction, Tischischenko-Claisen reaction, Tishchenko-Claisen reaction, Tishchenko–Claisen reaction, Tishischenko-Claisen reaction, Tishischenko–Claisen reaction.
