N-aizvietotu 2-aminomalonskābes monoesteru elektroķīmiska dekarboksilēšana iekšmolekulārā Hofera-Moesta reakcijā.
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Latvijas Universitāte
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lav
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N-Aizvietotu 2-aminomalonskābes monoesteru elektroķīmiska dekarboksilēšana iekšmolekulārā Hofera-Moesta reakcijā. Prāne K., Darba vadītāja MSc. chem. Koleda O. Bakalaura darbs ir uzrakstīts latviešu valodā, tā apjoms ir 50 lappuses. Darbs satur 16 attēlus, 10 tabulas, 39 literatūras avoti, 1 pielikums. Bakalaura darbā izstrādāta jauna elektroķīmiska N-aizvietotu 2-aminomalonskābes monoesteru dekarboksilēšanas metode, kurā notiek iekšmolekulāra ciklizācija. Izstrādātās reakcijas rezultātā iegūst otrajā pozīcijā ceturtējo oglekli saturošus tetrahidrofurānus un tetrahidropirānus. Iegūtie substrāti un produkti analizēti ar spektroskopijas metodēm.
Electrochemical decarboxylation of N-substituted 2-aminomalonic acid monoesters in intramolecular Hofer-Moest reaction. Prane K., supervisor MSc. chem. Koleda O. Bachelor’s thesis is written in Latvian and consists of 50 pages, 16 figures, 10 tables, 39 literature references, 1 appendices. A novel electrochemical decarboxylation of N-substituted 2-aminomalonic acid monoesters was developed. 2-Substituted tetrahydrofuranes and tetrahydropyranes, containing a quaternary carbon, are obtained in the developed reaction. The obtained compounds were characterized by using spectroscopic methods.
Electrochemical decarboxylation of N-substituted 2-aminomalonic acid monoesters in intramolecular Hofer-Moest reaction. Prane K., supervisor MSc. chem. Koleda O. Bachelor’s thesis is written in Latvian and consists of 50 pages, 16 figures, 10 tables, 39 literature references, 1 appendices. A novel electrochemical decarboxylation of N-substituted 2-aminomalonic acid monoesters was developed. 2-Substituted tetrahydrofuranes and tetrahydropyranes, containing a quaternary carbon, are obtained in the developed reaction. The obtained compounds were characterized by using spectroscopic methods.