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Titlebook: Herbicides Inhibiting Branched-Chain Amino Acid Biosynthesis; Recent Developments J. Stetter Book 1994 Springer-Verlag Berlin Heidelberg 19

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楼主: Opiate
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Mechanisms of Tolerance to Triazolopyrimidine Sulfonanilide Herbicides, at the whole plant level. Modifications in ALS can also impart tolerance. Evaluation of sulfonylurea and imidazolinone resistant weeds for sensitivity to triazolopyrimidines suggests greater likelihood of cross-resistance from sulfonylureas. A rapid method to identify target-site based resistance is described.
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Triazolopyrimidine Sulfonanilide Herbicides and Related Compounds,,5-.]pyrimidine, l,2,4-triazolo[l,5-.]-l,3,5-triazine, pyrazolo[l,5-.]-l,3,5-triazine and thiazolo[3,2-.]-l,2,4-triazole ring systems are included in this review. Aryl sulfonamide derivatives of 2-amino-l,2,4-triazolo[l,5-.]pyrimidine, 2-amino-l,2,4-triazolo[l,5-.]-l,3,5-triazine and 2-amino-l,2,4-pyrazolo- [l,5-.]pyrimidine are also covered.
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Recent Developments in the Chemistry of Sulfonylurea Herbicides,that has been developed to prepare a variety of sulfonamides, sulfonylureas with modified bridges, and sulfonylureas containing the sulfonylurea bridge fused to the heterocyclic portion of the molecule.
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Recent Developments in the Chemistry of Sulfonylurea Herbicides,ompanies. The importance of this class of herbicide, with their unprecedented levels of activity and the breadth of structural types, required the development of new synthetic methods in several chemical areas to enable the researcher to explore this class of herbicide. An in-depth review of the che
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Recent Advances in Sulfonylurea Herbicides, effort has led to the commercialization of 18 different active ingredients in over a dozen major crops, and additional development candidates have been announced. Some of the reasons for the rapid commercial acceptance of sulfonylurea herbicides include their exceptionally low application rates (of
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Recent Studies of Imidazolinone Herbicides and Related Compounds,l studies have provided novel derivatives and novel routes to new and existing analogs, and entry into the related series of compounds, the sulfonylcarboxamides. The newer structures have added to the understanding of structure-activity relationships, both in whole plants and at the enzyme level. Mo
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