| Autor: |
Nizamov, Ilyas S., Salikhov, Ramazan Z., Timushev, Ildus D., Nikitin, Yevgeniy N., Nizamov, Ilnar D., Yakimov, Vladimir Yu., Shulaeva, Marina P., Pozdeev, Oscar K., Batyeva, Elvira S., Cherkasov, Rafael A., Ponomareva, Anna S. |
| Předmět: |
|
| Zdroj: |
Phosphorus, Sulfur & Silicon & the Related Elements; 2020, Vol. 195 Issue 3, p226-230, 5p |
| Abstrakt: |
A new series of chiral carboxypyridinium dithiophosphates were synthesized by the reactions of nicotinic, isonicotinic, and picolinic acids with dithiophosphoric acid on the basis (1S)-endo-(–)-borneol in benzene or ethanol. 5,5-Dimethyl-2-mercapto-2-thiono-1,3,2-dioxaphosphorinane reacted with 3-hydroxypyridine or 3-pyridinemethanol in EtOH to afford the 3-hydroxypyridinium and 3-hydroxymethylpyridinium 5,5-dimethyl-2-mercapto-2-thiono-1,3,2-dioxaphosphorinanes which possessed antifungal activity against Candida albicans. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
|
