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Investigation of Synthesis of Functionally Substituted Endiines and Their Chemical and Microbiological Conversion

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DOI: 10.4236/ijoc.2013.33A002    2,312 Downloads   3,765 Views   Citations

ABSTRACT

The methods of preparation of endiine and endiallene diols by interaction of cis-1,4-dibrombutene and cis-1,4-dichlor-rbutene with monosubstituted acetylene alcohols in presence of the catalytic systems consisting of one-iodide copper, triethylamine and K2СО3 in a medium of dimethylformamide have been developed. It has been shown that unlike 1,4-dibrombutene, the nucleophilic substitution reaction with 1,4-dichlorbutene proceeds by acetylene-allene isomerization with formation of endiallene diols. It has been established that the endiine diols can be used in thin organic synthesis (in the reactions of oxidation, splitting, dehydration, epoxidation, hydrolysis, 1,2-cycloaddition and hypochlorination) with the aim of preparation of practically useful substances. It has been revealed during hydrolysis of epoxide compounds by the chemical and microbiological methods that in the course of microbiological hydrolysis (Aspеrgillus niger), the optically active trans-structured diols are formed.

Conflicts of Interest

The authors declare no conflicts of interest.

Cite this paper

M. Veliyev, M. Salmanov, M. Shatirova, S. Aliyeva and L. Bunyatova, "Investigation of Synthesis of Functionally Substituted Endiines and Their Chemical and Microbiological Conversion," International Journal of Organic Chemistry, Vol. 3 No. 3A, 2013, pp. 8-14. doi: 10.4236/ijoc.2013.33A002.

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