SYNTHESIS OF A FOSTEDIL ANALOG - DIETHYL 4-(1,2,3-DIDAZAPHOSPHOL-5-YL) BENZYLPHOSPHONATE - ANALYSIS OF ITS CALCIUM-TRANSPORT INHIBITING ACTIVITY THROUGH BIOLOGICAL-MEMBRANES
Yk. Rodi et al., SYNTHESIS OF A FOSTEDIL ANALOG - DIETHYL 4-(1,2,3-DIDAZAPHOSPHOL-5-YL) BENZYLPHOSPHONATE - ANALYSIS OF ITS CALCIUM-TRANSPORT INHIBITING ACTIVITY THROUGH BIOLOGICAL-MEMBRANES, Phosphorus, sulfur and silicon and the related elements, 85(1-4), 1993, pp. 225-231
We describe a four step synthesis of dicoordinated phosphorus Fostedil
analogues: the diethyl-4 (1,2,3-diazaphosphol-5-yl)benzylphosphonates
6, in which the benzothiazole Fostedil group is replaced by a 1,2,3 d
iazaphosphole ring. Inhibitive activity of calcium transfert, through
biological membranes, of compounds 6 is weak.