Synthesis and Fungicidal Activity of N-(Arylsulfonylaminoethyl)-1,6-caprolactam
WU Jing-ping
Abstract
WU Jing-ping
Abstract
Nine novel N-(arylsulfonylaminoethyl)-1,6-caprolactams(3) were synthesized from cyclohexanone.Their structures were confirmed by IR,1H NMR,13C NMR and elemental analysis.The bioassay showed that they have fungicidal activity against 6 kinds of fungi.Especially,the fungicidal activity of compounds 3a,3b,3d and 3g against Cladosporium graminis may be matched with that of commercial fungicide chlorothalonil.The inhibition rate was larger than 90%.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Nine novel N-(arylsulfonylaminoethyl)-1,6-caprolactams(3) were synthesized from cyclohexanone.Their structures were confirmed by IR,1H NMR,13C NMR and elemental analysis.The bioassay showed that they have fungicidal activity against 6 kinds of fungi.Especially,the fungicidal activity of compounds 3a,3b,3d and 3g against Cladosporium graminis may be matched with that of commercial fungicide chlorothalonil.The inhibition rate was larger than 90%.
Key concepts: Fungicide, Chlorothalonil, Cyclohexanone, Bioassay, Chemistry, Carbon-13 NMR, Proton NMR, Cladosporium