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Novel N-cyanoguanidyl derivatives: Synthesis and studying their toxicological activity against Spodoptera littoralis and Schizaphis graminum

A. Khodairy, Erian. S. Mansour, Omar M. Elhady, Ali M. Drar

2021Current Chemistry Letters18 citationsDOIOpen Access PDF

Abstract

Reaction of N-cyanoguanidine with acid chlorides and aroylisothiocyanates gave the respective; N-(N-cyanocarbamimidoyl)aryl-2-carboxamides 1-5 and N-[(N-cyanocarbamimidoyl)carbamothioyl]benzamides 6-10, which have a Neonictinoid insecticide’s active group moiety (=N–CN). They have more toxicological activity against wheat Aphid (Schizaphis graminum) than Spodoptera littoralis.

Topics & Concepts

Spodoptera littoralisChemistryAphidMoietyArylSpodopteraStereochemistryMedicinal chemistryOrganic chemistryBotanyBiochemistryNoctuidaePEST analysisBiologyGeneRecombinant DNAAlkylInsect-Plant Interactions and Control
Novel N-cyanoguanidyl derivatives: Synthesis and studying their toxicological activity against Spodoptera littoralis and Schizaphis graminum | Litcius