2007Journal of Heterocyclic ChemistryRequires access

Synthesis and herbicidal activities of a series of di(aminopyrazoly) ketone derivatives

Jun‐Fei Li, You‐Quan Zhu, Xin Wang, Hua‐Zheng Yang

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Abstract

Abstract magnified image In order to obtain new lead compounds with high herbicidal activity, a series of 5‐amino pyrazole derivatives were designed and synthesized using a series of relational synthons. Their structures were determined by IR, 1 H NMR, and elemental analyses. These compounds were screened for herbicidal activities against rape and barnyard grass. Their structure‐activity relationships are discussed.

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Abstract magnified image In order to obtain new lead compounds with high herbicidal activity, a series of 5‐amino pyrazole derivatives were designed and synthesized using a series of relational synthons. Their structures were determined by IR, 1 H NMR, and elemental analyses. These compounds were screened for herbicidal activities against rape and barnyard grass. Their structure‐activity relationships are discussed.

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Available abstract

Abstract magnified image In order to obtain new lead compounds with high herbicidal activity, a series of 5‐amino pyrazole derivatives were designed and synthesized using a series of relational synthons. Their structures were determined by IR, 1 H NMR, and elemental analyses. These compounds were screened for herbicidal activities against rape and barnyard grass. Their structure‐activity relationships are discussed.

Key concepts: Chemistry, Synthon, Ketone, Series (stratigraphy), Pyrazole, Stereochemistry, Proton NMR, Elemental analysis

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