Piperidine
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(Difference between revisions)
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* Stork-Enamine alkylation: http://en.wikipedia.org/wiki/Stork_enamine_alkylation | * Stork-Enamine alkylation: http://en.wikipedia.org/wiki/Stork_enamine_alkylation | ||
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| + | === Piperidine derivatives in nucleophilic ketol-enol (imine) substitutions === | ||
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| + | * For DNA depurination with a 2-cyanoethyl hetero-aryl-alkyl moeity (ie: a N-methyl cyanide anion), see [[Ethanamine]] | ||
| + | * For in situ polymer-based drug delivery of phenethylamine substituted imines, see [[Phenethylamine]] | ||
== See also == | == See also == | ||
* [[THF]] | * [[THF]] | ||
| + | * [[PVA]] | ||
| + | * [[PEA]] | ||
Revision as of 21:26, 19 February 2013
- An important secondary amine used as precursor to alkylamines with a aryl-ketone (heteroarylalkyl) moeity when the reaction is performed in presence of a cyanide as the nitrogen substitution group .
- In organic ketone-amine reactions, piperidine may participate in hydrogenation of C=N double bounds where the N-substituted chiral imine may be converted to a enamine, the tautomeric form of a imine. 1
Reductive alkylation of N-aryl substituted imines via piperidine-derived enamines
- Stork-Enamine alkylation: http://en.wikipedia.org/wiki/Stork_enamine_alkylation
Piperidine derivatives in nucleophilic ketol-enol (imine) substitutions
- For DNA depurination with a 2-cyanoethyl hetero-aryl-alkyl moeity (ie: a N-methyl cyanide anion), see Ethanamine
- For in situ polymer-based drug delivery of phenethylamine substituted imines, see Phenethylamine
