Zobrazeno 1 - 10
of 14
pro vyhledávání: '"H. L. Boter"'
Autor:
H. J. Toet, H. L. Boter
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 84:1279-1283
In this paper is described the preparation of some o- and m-nitrophenyl phosphates and phosphonates, m-dimethylaminophenyl phosphates and phosphonates, a S-p-nitrophenyl phosphorothiolate and a S-p-nitrophenyl phosphonothiolate. All the compounds exc
Autor:
H. L. Boter
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 87:957-960
Autor:
A. J. J. Ooms, H. L. Boter
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 85:21-30
A number of alkyl and cycloalkyl methylphosphonofluoridothionates were prepared by treatment of methylphosphonothioic difluoride with a mixture of one mole equivalent each of the appropriate alcohol and triethylamine in ether or benzene medium. React
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 85:147-150
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 87:387-395
The reaction of (+)-(i-PrO)MeP(O)SMe with phenylmagnesium bromide in tetrahydrofuran affords (+)-(i-PrO)MeP(O)Ph, representing the first example of a stereospecific synthesis of a phosphinate ester from a phosphonothiolate ester. Levorotatory (MeS)Me
Autor:
H. L. Boter, G. R. van den Berg
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 85:919-927
Some alkyl methylphosphonofluoridates were prepared by the reaction of the dicyclohexylamine salts of O-alkyl hydrogen methylphosphonothioates with 2,4,6-trinitrofluorobenzene in acetone solution. The mechanism of the reaction is discussed. The synth
Publikováno v:
International Journal of Environmental Analytical Chemistry. 21:63-77
Trace amounts (ppb or less) of phosphorus containing compounds present in aqueous samples are adsorbed on XAD-4 and subsequently eluted by means of ethyl acetate. The solvent and the eluted compounds are evaporated and swept over a Tenax-GC tube. Thi
Publikováno v:
Journal of Analytical Toxicology. 9:254-257
A procedure for the semi-quantitative determination of thiodiglycol, a metabolite of the vesicant mustard gas, in urine has been developed. Thiodiglycol was converted into mustard gas using concentrated HCl at temperatures close to 100 degrees C. The
Autor:
H. L. Boter, D. H. J. M. Platenburg
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 86:399-404
A series of four O-alkyl hydrogen methylphosphonothioates, (RO)MeP(S)OH, was resolved using both (+)- and (−)-α-phenylethylamine. Because it gives better results, is rapid and of general applicability the method is to be preferred to that in which
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1