Optimization of Osthole in the Lactone Ring: Structural Elucidation, Pesticidal Activities, and Control Efficiency of Osthole Ester Derivatives.

Abstract

Here, we prepared a series of novel osthole-type ester derivatives modified in the lactone ring of osthole, which is isolated from Cnidium monnieri. The positions of H-3 and H-4 of the representative compound 4z were determined by a 1H-1H COSY spectrum. By opening the lactone ring of osthole, the double bonds at the C-3 and C-4 positions of diol 3 and esters 4a-4z, 4a', and 4b' were still retained as a Z configuration. That is, H-3 and H-4 of compounds 3 and 4a-4z, 4a', and 4b' were all in the cis relationship. The steric configurations of 4k, 4v, and 4z were further undoubtedly determined by single-crystal X-ray diffraction. Against Tetranychus cinnabarinus Boisduval, four aliphatic esters 4c (R = n-C3H7; LC50: 0.31 mg/mL), 4d (R = CH3(CH2)10; LC50: 0.24 mg/mL), 4a' (R = CH3(CH2)9; LC50: 0.28 mg/mL), and 4b' (R = CH3(CH2)12; LC50: 0.32 mg/mL) showed the most promising acaricidal activity, and compounds 4c, 4d, and 4a' also exhibited a potent control efficiency. Especially, compound 4d exhibited greater than fivefold acaricidal activity of the precursor osthole (LC50: 1.22 mg/mL). Against Mythimna separata Walker, compounds 4g, 4l, and 4m displayed 1.6-1.8-fold potent insecticidal activity of osthole. It demonstrated that the lactone ring of osthole is not necessary for the agricultural activities, thiocarbonylation of osthole was not beneficial for the agricultural activities, introduction of R as an aliphatic chain is vital for the acaricidal activity, notably, the length of the aliphatic chain is related to the acaricidal activity, 4d could be further studied as a lead acaricidal agent, and to the aromatic series, R containing the fluorine atom(s) is important for the insecticidal activity.