Imine

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Broader Terms

organic base

Narrower Terms

Schiff base

Facts (generated by robot; please edit if you find it inaccurate)

  • A Catalyst for the Imino Aldol Reaction The asymmetric aldol reaction of an enolate or enolate equivalent with an imine is a reaction of established synthetic importance for the synthesis of chiral amines in general and b-amino esters in particular.
  • Be able to predict the products of a reaction in which an imine is formed.
  • The phenyl group makes the Schiff base a stable imine imine quick summary: An imine is a functional group or chemical compound containing a carbon-nitrogen double bond.
  • This facilitates bond scission because the protonated imine is more strongly electron-withdrawing than the carbonyl group, and the imine is easily protonated.
  • 2a,3a This model emphasized a six-membered transition state where the (Z)-imine is held together by N - H interactions from the proline carboxylic acid group to the forming amine.

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