| Autor: |
Kolomnikova, G. D., Prikhodchenko, D. Yu., Kuznetsova, S. A., Petrovskii, P. V., Kasukhin, L. F., Gololobov, Yu. G. |
| Zdroj: |
Russian Chemical Bulletin; February 1992, Vol. 41 Issue: 2 p337-341, 5p |
| Abstrakt: |
The vinyl esters of phosphorus acids containing an a-chloromethylalkenyl substituent react readily with thiourea to form substituted phosphorylated S-isothiuronium chlorides, capable of being dialkylated to the corresponding internal salts (betaines). An allylic rearrangement was discovered for the first time in the series of substituted S-isopropenylisothiuronium salts. The anticholinesterase and toxicological characteristics of some of the obtained comopunds were measured and compared. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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