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Synthesis of esters of metallocene alcohols and 4,5-dichloroisothiazol-3-carboxylic and 5-arylisoxazole-3-carboxylic acids

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Abstract

Acylation of alkyl- and 1,1′-dialkylferrocene alcohols and diols as well as (3,4,4-trichlorobut-3-ene-1-ol-1-yl)-4,5-cymantrene with dichloroisothiazole- and 5-arylisoxazole-3-carbonyl chlorides has afforded esters containing 1,2-azoles fragments. Some of the obtained compounds have exhibited potentiating action in the binary mixtures with insecticides.

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Correspondence to V. I. Potkin.

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Original Russian Text © V.I. Potkin, E.A. Dikusar, A.V. Kletskov, S.K. Petkevich, E.A. Semenova, I.A. Kolesnik, T.D. Zvereva, N.A. Zhukovskaya, I.B. Rosentsveig, G.G. Levkovskaya, R.M. Zolotar, 2016, published in Zhurnal Obshchei Khimii, 2016, Vol. 86, No. 2, pp. 310–316.

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Potkin, V.I., Dikusar, E.A., Kletskov, A.V. et al. Synthesis of esters of metallocene alcohols and 4,5-dichloroisothiazol-3-carboxylic and 5-arylisoxazole-3-carboxylic acids. Russ J Gen Chem 86, 338–343 (2016). https://doi.org/10.1134/S1070363216020237

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  • DOI: https://doi.org/10.1134/S1070363216020237

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