摘要:
Substituted triazole compounds, their preparation, compositions containing said compounds and the use of said compositions to control fungal infections in plants are disclosed.
摘要:
Substituted azole compounds especially substituted imidazole and triazole compounds, their preparation, compositions containing said compounds and the use of said compositions to control fungal infections in plants are disclosed.
摘要:
Embodiments relate to the field of chemistry and biochemistry, and, more specifically, to imidazopyridine compounds, synthesis thereof, and methods of using same. Disclosed herein are various imidazo[1,2-a]pyhdine compounds and methods of using the novel compounds to treat or prevent tuberculosis in a subject or to inhibit fungal growth on plant species. Other embodiments include methods of synthesizing imidazo [1,2- a]pyridine compounds, such as the disclosed imidazo[1,2-a]pyridine compounds.
摘要:
A process for the dehydrohalogenation of a (polyhaloalkyl)benzene containing a benzylic halogen such as 1,3-dichloro-5-(2,4,4,4-tetrachlorobutyl)benzene by contacting the (polyhaloalkyl)benzene with a suitably active Lewis acid catalyst such as SbCl.sub.5 or TiCl.sub.4 under conditions sufficient to catalyze said dehydrohalogenation to form a (polyhaloalkenyl)benzene such as 3,5-dichloro-.alpha.-(2,2,2-trichloroethyl)styrene.
摘要:
In an isomeric mixture of ar-substituted-1-(sec-alkyl)benzenes, such as a mixture of 2-chlorocumene, 3-chlorocumene and 4-chlorocumene, the alkyl groups of the 3-isomer and 4-isomer react preferentially with a halogen in the presence of a catalyst such as benzoyl peroxide to form a 3-halo-1-(.alpha.-alkyl, .alpha.-halo)alkylbenzene and 4-halo-1-(.alpha.-alkyl, .alpha.-halo)alkylbenzene such as 3-chloro-.alpha.-bromocumene, and 4-chloro-.alpha.-bromocumene.
摘要:
In a mixture of isomers of ar,ar-dihalo-ar-alkylbenzene wherein the halogen substituents are meta oriented with respect to each other, (e.g., a mixture of 3,5-dichlorocumene and 2,4-dichlorocumene), the 2,4-dihalo-1-alkylbenzene is preferentially reacted with an alkylating agent, e.g., an alkyl halide, by contacting the mixture with the agent in the presence of a Friedel-Crafts catalyst at a temperature of less than about 90.degree. C. The resulting alkylated isomer is readily separated from the unreacted isomer(s) by simple distillation.
摘要:
4-Substituted 5-polycyclylpyrimidine compounds in which the 5-substituent is polycyclic and is attached to the pyrimidine moiety through an aliphatic carbon atom, such as 5-(2,2-dimethylindan-1-yl)-4-methylthiopyrimidine, were prepared and found to possess excellent herbicidal activity. The compounds are especially useful for the control of undesirable vegetation in paddy rice.
摘要:
The herbicidal action of a herbicidal triazine upon weeds is enchanced upon also applying to the weeds a second herbicidal component, a butyl or pentyl glycol sulfonate or glycol sulfamate having 3, 5 or 3 substituted phenyl in the 2-position of the butyl or pentyl chain. The glycol sulfonate or sulfamate also adds its own herbicidal action to increase effectiveness.Both components are applied simultaneously as a novel composition which may also contain crop oil or crop oil concentrate. Application is made post-emergently before weeds reach about the 8 leaf stage. Advantageously, in an additional step, triazine alone or in combination with at least some of the sulfonate or sulfamate is also applied at planting or very early postemergently prior to the treatment described.
摘要:
Sulfur-substituted phenoxypyridines having antiviral activity are disclosed. Methods of using the sulfur-substituted phenoxypyridines to employ their antiviral activity are also disclosed as well as pharmaceutically-acceptable compositions thereof.