Synthesis and Biological Activity of 3- and 4-Aminomethyl-1,2-dithiolanes

概要

論文の詳細を見る
The structures of the insecticidal alkaloids, guinesines (4-hydroxy-3-(1-methyl-2-pyrrolidinyl)-1,2-dithiolanes), were simplified in several ways while retaining the dithiolane ring. Most of the compounds synthesized showed activity against Chilo suppressalis and Tetranychus urticae. High potency against Chilo suppressalis was displayed by 3-(dimethylaminomethyl)-1,2-dithiolane, and a broad pesticidal spectrum was recognized in the case of 4-(dimethylaminomethyl)-1,2-dithiolane.
社団法人日本農芸化学会の論文
1992-08-23