118876-86-1Relevant articles and documents
Novel synthesis of 4(5)-monosubstituted imidazoles via cycloaddition of tosylmethyl isocyanide to aldimines
Ten Have, Ronald,Huisman, Marco,Meetsma, Auke,Van Leusen, Albert M.
, p. 11355 - 11368 (1997)
4(5)-Monosubstituted imidazoles (9) have been prepared via base-induced cycloaddition of tosylmethyl isocyanide (TosMIC) to N-(dimethylsulfamoyl)aldimines (2) or N-tosylaldimines (3). In the first case, N-(dimethylsulfamoyl)imidazoles 8 are the initial reaction products, from which the dimethylsulfamoyl group is readily removed with aqueous HBr. In the second case, the tosyl group of 1-tosylimidazoles 10 is lost spontaneously to give 4(5)-monosubstituted imidazoles 9 in one operation.
Imidazable fungicides and use thereof
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, (2008/06/13)
The invention provides compounds of formula I STR1 in which X, R1, R2 and R3 are as defined in the description. The compounds have valuable fungicidal activity.
Cyanoimidazole fungicides
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, (2008/06/13)
The invention provides compounds of formula I in which X, R1, R2 and R3 are as defined in the description. The compounds have valuable fungicidal activity