SYNTHESIS AND BIOLOGICAL ACTIVITY OF α-ALKYLACROLEIN DIMERS AND THEIR DERIVATIVES

Authors

  • Н. М. Карпяк Lviv National Polytechnic University, Lviv 79013
  • Г. А. Маршалок Lviv National Polytechnic University, Lviv 79013
  • М. Д. Федевич Lviv National Polytechnic University, Lviv 79013
  • И. К. Авдосьева State Scientific Research Control Institute of Veterinary Preparations and Fodder Additives, Lviv 79019
  • Я. П. Ковальский Lviv National Polytechnic University, Lviv 79013

DOI:

https://doi.org/10.1007/7275

Keywords:

2, 5-dimethyl-3, 4-dihydro-2H-pyran-2-carbaldehyde, 4-dihydro-2H-pyran-2-methanol, 5-diethyl-3, sodium salts of 2, 4-dihydro-2H-pyran-2-carboxylic and 2, 4-dihydro-2H-pyran-2-carboxylic acids, Diels-Alder reaction, Cannizzaro reaction

Abstract

Dimers of methacrolein and α-ethylacrolein have been obtained and undergo a Cannizzaro reaction to the corresponding pyran alcohols and sodium salts of  pyran acids. Their bacteriostatic, bactericidal, and fungicidal properties have been studied.

How to Cite
Karpiak, N. M.; Marshalok, H. A.; Fedevich, M. D.; Avdosieva, I. K.; Kovalskyi, Ya. P.  Chem. Heterocycl. Compd. 2008, 44, 1334. [Khim. Geterotsikl. Soedin. 2008, 1639.]

For this article in the English edition see DOI 10.1007/s10593-009-0200-3

 

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Published

2023-01-03

Issue

No. 11 (2008)

Section

Original Papers