Reactions of phosphorylated 2,6-di- tert -butyl-4-methylidenecyclohexa-2,5-dien-1-ones with aliphatic, aromatic, and heteroaromatic thiols

M. B. Gazizov; A. L. Pistsova; R. K. Ismagilov; L. P. Shamsutdinova; R. F. Karimova; R. N. Burangulova

doi:10.1134/S107036321705036X

Reactions of phosphorylated 2,6-di-tert-butyl-4-methylidenecyclohexa-2,5-dien-1-ones with aliphatic, aromatic, and heteroaromatic thiols

Autores: Gazizov M.¹, Pistsova A.¹, Ismagilov R.¹, Shamsutdinova L.¹, Karimova R.¹, Burangulova R.¹
Afiliações:
1. Kazan National Research Technological University
Edição: Volume 87, Nº 5 (2017)
Páginas: 1101-1103
Seção: Letters to the Editor
URL: https://journals.rcsi.science/1070-3632/article/view/220103
DOI: https://doi.org/10.1134/S107036321705036X
ID: 220103

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The addition of alkanethiols, benzenethiol, and hetarenethiols to phosphorylated quinomethanes afforded P,S- and N,P,S-containing polyfunctional organic compounds as potential bactericidal agents.