User:Etienne Robillard/Notebook/Schiff base
From OpenWetWare
(Difference between revisions)
(Added a reference about PD link to THIQ.) |
(→Formation of phenylmethylamine as the tautomeric form of a ethyl-methyl carbanion) |
||
| Line 7: | Line 7: | ||
* 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. | * 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 disease relevance of Parkinson disease as the result of prolonged 1,2,3,4-tetrahydroisoquinolines derivatives absorption: A 2-phenylmethylamine-specific enatiomer ? | + | * assert disease relevance of Parkinson disease [2] as the result of prolonged 1,2,3,4-tetrahydroisoquinolines derivatives absorption: A 2-phenylmethylamine-specific enatiomer ? |
=== References === | === References === | ||
Revision as of 08:37, 27 February 2013
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. [1]
- 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 disease relevance of Parkinson disease [2] as the result of prolonged 1,2,3,4-tetrahydroisoquinolines derivatives absorption: A 2-phenylmethylamine-specific enatiomer ?
