User:Etienne Robillard/Notebook/Schiff base
< User:Etienne Robillard | Notebook
Introduction to Schiff bases
- Insert text here in scientifically acceptable way (ie: without grammar errors) to explain the functions and basics of Schiff base formation. 
- Present summarly the basic psychopharmacological aspects/functions of imine in a biological system .
Formation of phenylmethylamine as the tautomeric form of a ethyl-methyl carbanion
- For the long story, see Phenylmethylamine: A nucleophilic Schiff base where the N-substituted anion is fused to a benzene ring (?) to yield a enamine. See also Ethanamine. Note that the C=N double bond is the result (product) of asymmetric synthesis (Micheal addition) in presence of a organometal catalyst.
- assert biological relevance of Parkinson disease  as the result of prolonged 1,2,3,4-tetrahydroisoquinolines derivatives absorption: A 2-phenylmethylamine-specific enatiomer ?