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Spirodiclofen Analogues as Potential Lipid Biosynthesis Inhibitors: A Convenient Synthesis, Biological Evaluation, and Structure-Activity Relationship
Twenty spirodiclofen analogues have been designed and conveniently synthesized via three steps including esterification,one-pot heterocyclization, and acylation reactions. The target molecules have been identified on the basis of analytical spectra (1H NMR, 13C NMR and ESI-MS) data. All newly synthe...
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Published in: | Bulletin of the Korean Chemical Society 2010, 31(8), , pp.2315-2321 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Twenty spirodiclofen analogues have been designed and conveniently synthesized via three steps including esterification,one-pot heterocyclization, and acylation reactions. The target molecules have been identified on the basis of analytical spectra (1H NMR, 13C NMR and ESI-MS) data. All newly synthesized compounds have been screened for their potential insecticidal and herbicidal activity by standard method. The preliminary assays indicated that some of analogues displayed moderate to good insecticidal activity against Plutella xylostella compared with spirodiclofen,and some compounds showed obvious activity against Brassica chinensis. Structure-activity relationship (SAR) is also discussed based on the experimental data. KCI Citation Count: 9 |
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ISSN: | 0253-2964 1229-5949 |
DOI: | 10.5012/bkcs.2010.31.8.2315 |