| Title : Easy access to phosphonothioates - Renard_2002_Chemistry_8_2910 |
| Author(s) : Renard PY , Schwebel H , Vayron P , Josien L , Valleix A , Mioskowski C |
| Ref : Chemistry , 8 :2910 , 2002 |
|
Abstract :
A new and particularly mild method for the formation of phosphorus-sulfur bonds has been achieved through base-catalyzed addition of thiocyanate to the corresponding H-phosphine oxide, phosphinate, or phosphonate. This reaction procedure offers many advantages: the use as starting material of a stable and not oxygen-sensitive phosphorus(v) species, particularly mild and nonaqueous reaction conditions and workup (a pivotal point for these sensitive phosphonothioates), and, through optimized access to thiocyanates, a wider scope of substrates. This method has been applied to achieve the synthesis of substrate analogues for the study of antibody-catalyzed hydrolysis of acetylcholinesterase inhibitor PhX (11). |
| PubMedSearch : Renard_2002_Chemistry_8_2910 |
| PubMedID: 12489219 |
| Inhibitor | PhX |
Renard PY, Schwebel H, Vayron P, Josien L, Valleix A, Mioskowski C (2002)
Easy access to phosphonothioates
Chemistry
8 :2910
Renard PY, Schwebel H, Vayron P, Josien L, Valleix A, Mioskowski C (2002)
Chemistry
8 :2910