The thionophosphate–thiolophosphate † photoisomerization proceeds predominantly through a non-chain radical pathway. Synthetically viable benzylation of tetrahydrofuran, propan-2-ol and olefins ‡
The thionophosphate–thiolophosphate † photoisomerization proceeds predominantly through a non-chain radical pathway. Synthetically viable benzylation of tetrahydrofuran, propan-2-ol and olefins ‡
The Kinetics of the base hydrolyses of a series of α-cyano thiophosphate esters are presented. A classic Hammett sigma-rho analysis showed these hydrolyses to be bimolecular in nature.
The reaction between phosphorothioic and thiocarboxylic acids and O-alkyl-N,N-dicyclohexylisoureas has been found to give the corresponding phosphorothiolates and thiolocarboxylates in high yields (65-95%), providing a new method for the thiophosphorylation and thiocarboxylation of alcohols.