Piperidine
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(Difference between revisions)
(New page: An important secondary amine used as precursor to alkylamines with a [http://en.wikipedia.org/wiki/Piperidine#Reactions aryl-ketone] (heteroarylalkyl) moeity when the reaction is performed...) |
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| - | An important secondary amine used as precursor to alkylamines with a [http://en.wikipedia.org/wiki/Piperidine#Reactions aryl-ketone] (heteroarylalkyl) moeity when the | + | * An important secondary amine used as precursor to alkylamines with a [http://en.wikipedia.org/wiki/Piperidine#Reactions aryl-ketone] (heteroarylalkyl) moeity when the |
reaction is performed in presence of a cyanide as the nitrogen substitution group . | 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 http://en.wikipedia.org/wiki/Hydrogenation_of_carbon-nitrogen_double_bonds] where | ||
| + | the N-substituted chiral imine may be converted to a enamine, the tautomeric form of a imine. [1] | ||
| + | |||
| + | == See also == | ||
| + | |||
| + | * [[THF]] | ||
Revision as of 08:10, 17 January 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 http://en.wikipedia.org/wiki/Hydrogenation_of_carbon-nitrogen_double_bonds] where
the N-substituted chiral imine may be converted to a enamine, the tautomeric form of a imine. [1]
