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

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

doi:10.1134/S1070363216020237

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

Autores: Potkin V.¹, Dikusar E.¹, Kletskov A.¹, Petkevich S.¹, Semenova E.¹, Kolesnik I.¹, Zvereva T.¹, Zhukovskaya N.¹, Rosentsveig I.², Levkovskaya G.², Zolotar R.³
Afiliações:
1. Institute of Physical Organic Chemistry
2. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
3. Institute of Bioorganic Chemistry
Edição: Volume 86, Nº 2 (2016)
Páginas: 338-343
Seção: Article
URL: https://journals.rcsi.science/1070-3632/article/view/213834
DOI: https://doi.org/10.1134/S1070363216020237
ID: 213834

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Resumo

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.