15367-75-6Relevant articles and documents
A study of the effect of the nature of the solvent and temperature on the route of the reaction of thiobenzyl esters of PIII acids with molecular oxygen
Drozdova, Ya. A.,Burilov, A. R.,Pudovik, M. A.
, p. 1379 - 1381 (1993)
The effects of the nature of the solvents, the degree of dilution, the duration of the process, and the temperature on the ratio of the products obtained in the reactions of S-benzyl diphenylthiophosphinite or S,S-dibenzyl phenyldithiophosphonite with molecular oxygen have been studied.Possible reaction schemes are discussed. - Key words: thiobenzyl esters of PIII acids; solvents; degree of dilution; isomerization; phosphoranyl radicals, radical ions; complexes.
Ph2PI as a reduction/phosphination reagent: Providing easy access to phosphine oxides
Wang, Feijun,Qu, Mingliang,Chen, Feng,Xu, Qin,Shi, Min
, p. 8580 - 8582 (2012/09/22)
The reaction of aldehydes with Ph2PI provides a facile way to the synthesis of pentavalent phosphine compounds with moderate to good yields.
PHASE-TRANSFER CATALYTIC ALKYLATION OF HYDROTHIOPHOSPHORYL COMPOUNDS. IV. REACTIONS WITH PRIMARY ALKYL HALIDES
Aladzheva, I. M.,Odinets, I. L.,Petrovskii, P. V.,Mastryukova, T. A.,Kabachnik, M. I.
, p. 431 - 437 (2007/10/02)
A convenient general method for the synthesis of compounds containing a thiophosphoryl group was elaborated on the basis of the Michaelis-Becker reaction with the use of the method of phase-transfer catalysis. The influence of the nature of the hydrothiophosphoryl compounds, of the alkylating agents, and of the reaction conditions on the yields of alkylated products was investigated in detail.
