- Methods for Producing Sulfonic Acid Diamides
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The present invention relates to a process for preparing sulfuric diamides of the general formula I [in-line-formulae]R1R2N—S(O)2—NH2??(I)[/in-line-formulae] in which R1 and R2 are each ind
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Page/Page column 5
(2010/09/07)
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- Cyclopropyl Fused Indolobenzazepine HCV NS5B Inhibitors
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The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and may be useful in treating those infected with HCV.
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Page/Page column 58
(2010/09/05)
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- CYCLOPROPYL FUSED INDOLOBENZAZEPINE HCV NS5B INHIBITORS
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The invention encompasses compounds of formula (I) as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and are useful in treating those infected with HCV
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Page/Page column 72
(2009/06/27)
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- Cyclopropyl Fused Indolobenzazepine HCV NS5B Inhibitors
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The invention encompasses compounds of formula I as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and are useful in treating those infected with HCV.
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Page/Page column 52
(2008/06/13)
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- Uracil substituted phenyl sulfamoyl carboxamides
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Novel uracil substituted phenyl sulfamoyl carboxamides I and salts thereof, where A=oxygen or sulfur; X1=H, halogen, C1-C4-alkyl; X2=H, CN, CS—NH2, halogen, C1-C4-alkyl, C1-C4-haloalkyl; X3=H, CN, C1-C6-alkyl, C1-C6-alkoxyalkyl, C3-C7-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, optionally substituted benzyl; R1, R2=H, halogen, optionally substituted hydroxy, C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkynyl, C3-C7-cycloalkyl, phenyl, benzyl or C5-C7-cycloalkenyl, or R1+R2 together with the atom to which they are attached form a 3- to 7-membered heterocyclic ring; Q is selected from Q1 to Q40 as defined in the description. Use: As herbicides; for the desiccation/defoliation of plants.
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