SYNTHESIS AND FUNGICIDAL ACTIVITY OF METHYLSULFANYLMETHYL ETHER DERIVATIVES OF LEVOGLUCOSENONE
DOI:
https://doi.org/10.1007/4860Keywords:
γ-butanolides, levoglucosenone, methylthiomethyl ethers, fungicidal activity, Rhizoctonia solaniAbstract
A series of derivatives were synthesized on the basis of levoglucosenone that contained hydroxy groups at the С-4 atom or С-2 and С-4 atoms or a hydroxy and methyl group at the С-4 atom. In addition, 4-hydroxymethylbutanolides were synthesized. Derivatives containing hydroxy groups were obtained as methylsulfanylmethyl ethers. It was established that compounds containing a 6,8-dioxabicyclo[3.2.1]octane ring exhibited fungicidal activity against Rhizoctonia solani. It was shown that the presence of a methylsulfanylmethyl moiety in the ring could increase the fungicidal activity of compounds.
Authors: Bulat T. Sharipov*, Anna N. Davidova, Alena S. Ryabova, Nailya F. Galimzyanova, Farid A. Valeev