Reactions of keto alcohols with organophosphorus compounds

Autor: Mukhametov, F. S., Stepashkina, L. V., Rizpolozhenskii, N. I.
Zdroj: Russian Chemical Bulletin; May 1977, Vol. 26 Issue: 5 p1040-1044, 5p
Abstrakt: Conclusions Reaction of ß-keto alcohols with amidophosphorous acid chlorides in the presence of triethylamine leads to the corresponding ?-ketoalkyl phosphate. The presence of electron-donor (dialkylamide) groups attached to the phosphorus atom in the ?-ketoalkyl phosphite products inhibits their spontaneous isomerization to ?-ketoalkylphosphonates. Phosphates and thiophosphates with ?-ketoalkyl radicals decompose to an a,ß-unsaturated ketone and the corresponding phosphorus acid.
Databáze: Supplemental Index