User:Etienne Robillard/Notebook/Piperidine

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(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
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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
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 .
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* 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
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the N-substituted chiral imine may be converted to a enamine, the tautomeric form of a imine. [1]
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== See also ==
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* [[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 .

the N-substituted chiral imine may be converted to a enamine, the tautomeric form of a imine. [1]

See also

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