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S. Pedragosa-Morean, A. Archelas and R. Furstoss, “Microbiological Transformations. 28. Enantiocomple- mentery Epoxide Hydrolyses as a Preparative Access to Both Enantiomers of Styrene Oxide,” Journal of Organic Chemistry, Vol. 58, No. 20, 1993, pp. 5533-5536. doi:10.1021/jo00072a044

has been cited by the following article:

• TITLE: Chemical and Microbiological Hydrolysis of Epoxides of Acetylene Series

  AUTHORS: Mammad Veliyev, Mammad Salmanov, Saida Aliyeva, Mahruza Shatirova, Gulnara Yagubova

  KEYWORDS: Hydrolyze, Glycols, Epoxide, Ketoalcohols, Acetylene

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.1 No.3, September 28, 2011

  ABSTRACT: The chemical and microbiological hydrolyses of epoxide compounds of acetylene series have been comparatively carried out. It has been shown that as distinguished from chemical one in microbiological hydrolysis along with corresponding optically active glycols, ketoalcohols of acetylene series are also formed. It has been also defined that the synthesized glycols of acetylene series have bactericide properties related to sulfate-reducing bacteria at concentration of 100 - 200 mg/l. It has been established that an introduction of electron-acceptor chlorine atoms in molecules influence on decreasing of bactericide activity of acetylene glycols.