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

Authors: Gazizov M.B.¹, Pistsova A.L.¹, Ismagilov R.K.¹, Shamsutdinova L.P.¹, Karimova R.F.¹, Burangulova R.N.¹
Affiliations:
1. Kazan National Research Technological University
Issue: Vol 87, No 5 (2017)
Pages: 1101-1103
Section: 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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Abstract

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.