| Title : Synthesis and characterization of the enantiomerically pure cis- and trans-2,4-dioxa-3-fluoro-3-phosphadecalins as inhibitors of acetylcholinesterase - Wachter_2009_Chem.Biodivers_6_283 |
| Author(s) : Wachter M , Ruedi P |
| Ref : Chem Biodivers , 6 :283 , 2009 |
|
Abstract :
The title compounds, the P(3)-axially- and P(3)-equatorially-substituted cis- and trans-configured 3-fluoro-2,4-dioxa-3-phosphadecalin 3-oxides (=3-fluoro-2,4-dioxa-3-phosphabicyclo[4.4.0]decane 3-oxides) have been prepared (ee>99%) and fully characterized. The compounds are irreversible inhibitors of acetylcholinesterase, and both the kinetic data and the mechanisms of the inhibition are determined by a novel enzyme-kinetic approach that is described in the preceding report. The inhibitors display pronounced stereoselectivity, and several of them are significantly stronger than diisopropyl fluorophosphate that is generally used as a potent standard. |
| PubMedSearch : Wachter_2009_Chem.Biodivers_6_283 |
| PubMedID: 19319864 |
Wachter M, Ruedi P (2009)
Synthesis and characterization of the enantiomerically pure cis- and trans-2,4-dioxa-3-fluoro-3-phosphadecalins as inhibitors of acetylcholinesterase
Chem Biodivers
6 :283
Wachter M, Ruedi P (2009)
Chem Biodivers
6 :283