61035-31-2Relevant academic research and scientific papers
α,β-UNSATURATED THIO COMPOUNDS. REDUCTION OF 3-HETEROSUBSTITUTED 2-ARYL-1-INDENETHIONES
Petriashvili, K. A.,Usov, V. A.,Protasova, L. E.,Shagun, V. A.,Sidorkin, V. F.,Voronkov, M. G.
, p. 513 - 517 (2007/10/02)
3-Amino-, 3-mercapto-, and 3-alkylthio-substituted 2-aryl-1-indenethiones react readily with sodium borohydride or S-nucleophiles, forming 2-aryl-3-indenethiols. 2-Phenyl-3-indenethiol in the thioketone tautomeric form is reduced by cyanide ion in DMFA to
α,β-UNSATURATED THIO COMPOUNDS. SYNTHESIS AND SOME CHEMICAL TRANSFORMATIONS OF THE THIO DERIVATIVES OF 2-ARYL-1-INDANONES AND 2-ARYL-1,3-INDANEDIONES
Petriashvili, K. A.,Usov, V. A.,Voronkov, M. G.
, p. 507 - 512 (2007/10/02)
In the reaction of 2-aryl-1-indanones and 2-aryl-1,3-indanediones with hydrogen sulfide in the presence of hydrogen chloride 2-aryl-3-indenethiols and 3-mercapto-2-aryl-1-indenethiones respectively are formed.The latter are readily acylated, condense with
