Musilek_2007_Molecules_12_1755

Reference

Title : Two step synthesis of a non-symmetric acetylcholinesterase reactivator - Musilek_2007_Molecules_12_1755
Author(s) : Musilek K , Kuca K , Dohnal V , Jun D , Marek J , Koleckar V
Ref : Molecules , 12 :1755 , 2007
Abstract :

The newly developed and very promising acetylcholinesterase reactivator (E)-1-(2-hydroxyiminomethylpyridinium)-4-(4-hydroxyiminomethylpyridinium)-but-2-e ne dibromide was prepared using two different pathways via a two-step synthesis involving the appropriate (E)-1-(4-bromobut-2-enyl)-2- or 4-hydroxyiminomethyl-pyridinium bromides. Afterwards, purities and yields of the desired product prepared by both routes were compared. Finally, its potency to reactivate several nerve agent-inhibited acetylcholinesterases was tested.

PubMedSearch : Musilek_2007_Molecules_12_1755
PubMedID: 17960085

Related information

Citations formats

Musilek K, Kuca K, Dohnal V, Jun D, Marek J, Koleckar V (2007)
Two step synthesis of a non-symmetric acetylcholinesterase reactivator
Molecules 12 :1755

Musilek K, Kuca K, Dohnal V, Jun D, Marek J, Koleckar V (2007)
Molecules 12 :1755