Pesticide Science p. 253 - 264 (1994)
Update date:2022-07-29
Topics:
Pascual, Alfons
Rindlisbacher, Alfred
In the course of optimization studies around diafenthiuron, the central aromatic nucleus linked directly to the thiourea unit was replaced by a pyridine moiety. A series of N-(pyrid-3-yl)thioureas, isothioureas and -carbodiimides was synthesised and evaluated for acaricidal activity. The synthetic methodology used and the screening results against some spider mites (Tetranychus spp. and Panonychus ssp.) are discussed.
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