Hagedorn_1976_Arzneimittelforschung_26_1515

Reference

Title : [Reactivation of phosphorylated acetylcholinesterase (AChE): quaternary salts of vinylogous pyridinaldoxims (author's transl)]. [German] - Hagedorn_1976_Arzneimittelforschung_26_1515
Author(s) : Hagedorn I , Hohler W
Ref : Arzneimittelforschung , 26 :1515 , 1976
Abstract :

Application of Wittig reaction to 4-pyridinecarboxaldehyde leads to 4-beta-formylvinylpyridine (62%). The corresponding oxime (4-(2)) can be quaternized with alpha,alpha'-bis-(chloromegonin), and with methyliodide one to 4-PAM (4-(3)). In this case the formal insertion of an ethylenic double bond between the pyridinium ring and the aldoxime group decreases the ability to reactivate phosphorylated acetylcholinesterase (AChE).

PubMedSearch : Hagedorn_1976_Arzneimittelforschung_26_1515
PubMedID: 1036947

Related information

Citations formats

Hagedorn I, Hohler W (1976)
[Reactivation of phosphorylated acetylcholinesterase (AChE): quaternary salts of vinylogous pyridinaldoxims (author's transl)]. [German]
Arzneimittelforschung 26 :1515

Hagedorn I, Hohler W (1976)
Arzneimittelforschung 26 :1515