| dc.contributor.advisor | Sūna, Edgars | en_US |
| dc.contributor.author | Vikainis, Sergejs | en_US |
| dc.contributor.other | Latvijas Universitāte. Ķīmijas fakultāte | en_US |
| dc.date.accessioned | 2015-03-24T08:22:10Z | |
| dc.date.available | 2015-03-24T08:22:10Z | |
| dc.date.issued | 2012 | en_US |
| dc.identifier.other | 22515 | en_US |
| dc.identifier.uri | https://dspace.lu.lv/dspace/handle/7/22854 | |
| dc.description.abstract | Darbā tika izstrādātas jaunas N-karbamoilmetil-4R-fenil-2-oksopirolidīna iegūšanas metodes, alkilējot (R)-fenil-4-aminosviestskābes n-butilesteri un ciklizējot ieguto starproduktu. N-Acetil-2-oksopirolidīna C3, C4 un C5 aizvietoto atvasinājumu bromēšanas reakcijas izpētes rezultātā tika izolēti un noraksturoti līdz šim neaprakstīti attiecīgie 1-acetil-4-fenil-3-pirolīn-2-oni, kā arī to 5-brom un 5,5-dibromatvasinājumi. | en_US |
| dc.description.abstract | Developement of new methods of N-carbamoylmethyl-4R-phenyl-2-oxopyrrolidine preparation by the alkylation of 3R-phenyl-4-aminobutyric acid n-butyl ester and by the cyclization of intermediate. The subjection of N-acetyl-2-oxopyrrolidine C3, C4 and C5 substituted derivatives to bromation and investigation of reaction products products resulted in the discovery of still unknown 1-acetyl-4-phenyl-3-pyrrolyn-2-ones the same as their 5-brom or 5,5-dibrom derivatives. | en_US |
| dc.language.iso | N/A | en_US |
| dc.publisher | Latvijas Universitāte | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Ķīmija | en_US |
| dc.title | 4-Fenil-2-oksopirolidīna ķīmisko īpašību pētīšana | en_US |
| dc.title.alternative | The investigation of 4-phenyl-2-oxopyrrolidine chemical properties | en_US |
| dc.type | info:eu-repo/semantics/masterThesis | en_US |
