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1.2.5- Thiadiazoles hydrocarbons

The reaction of active hydrocarbons, phenols, and related compounds with tetrasulfur tetranitride affords fused thiadiazoles, and this chemistry is well documented in CHEC(1984) <1984CHEC(6)513> and CHEC-II(1996) <1996CHEC-II(4)355>. No recent work has been reported. [Pg.551]

Sulfur nitride (N4S4) reacts with ethyl-substituted aromatic hydrocarbons forming aryl thiadiazoles. While the yields are low (6-12 %) the method is of value because of the simplicity of the organic starting... [Pg.123]

Amino-l,2,4-thiadiazoles can be diazotized with sodium nitrite in acetic acid because of the strong electron attraction of the l,2,4-thiadiazol-5-yl moiety and the resulting diazonium ions are highly electrophilic. They can even couple with the hydrocarbon mesitylene ... [Pg.199]

F3 14 Lipid peroxidation (prop.) Aromatic hydrocarbons/ thiadiazoles Biphenyl chloroneb/ etridiazole Diverse activity spectra... [Pg.428]

See other pages where 1.2.5- Thiadiazoles hydrocarbons is mentioned: [Pg.38]    [Pg.102]    [Pg.114]    [Pg.124]    [Pg.366]    [Pg.5226]   
See also in sourсe #XX -- [ Pg.24 , Pg.364 ]



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1,3,4-Thiadiazol

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