Renard_2002_Chemistry_8_2910

Reference

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

Related information

Inhibitor PhX

Citations formats

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