Selective reduction of C=C double bond of the Lactone ring - Bidar, Morteza
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The aim of the current work is development of the novel methods for the selective reduction of the double bond of lactone ring in 3-substituted 2-oxo-2,5-dihydrofurans and 2-oxo-5,6-dihydropyrns, as well as the synthesis of new derivatives of unsaturated -lactones on the basis of relatively accessible compounds of butenolide class, with the aim of searching for the biological activity among the synthesized structures.Two reducing systems -"magnesium-methanol" and "sodium borohydride-triethylamine" - are proposed for the selective reduction of C=C double bond of the lactone ring.

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Produktbeschreibung
The aim of the current work is development of the novel methods for the selective reduction of the double bond of lactone ring in 3-substituted 2-oxo-2,5-dihydrofurans and 2-oxo-5,6-dihydropyrns, as well as the synthesis of new derivatives of unsaturated -lactones on the basis of relatively accessible compounds of butenolide class, with the aim of searching for the biological activity among the synthesized structures.Two reducing systems -"magnesium-methanol" and "sodium borohydride-triethylamine" - are proposed for the selective reduction of C=C double bond of the lactone ring.
Autorenporträt
Dr. Morteza Bidar worked for his Ph.D. with research on " Selective reduction of C=C double bond of the lactone ring and the synthesis of the new derivatives of unsaturated ¿-lactone" at Yerevan state university in Armenia.