magistrsko delo
Abstract
V magistrskem delu so predstavljeni 2H-piran-2-oni, različne sintezne poti in njihova reaktivnost v različnih reakcijah. Ena izmed možnih pretvorb je preko cikloadicijskih reakcij, ki vodijo do zanimivih biciklo[2.2.2]oktenskih sistemov. V eksperimentalnem delu sem se posvetila reakcijam 2H-piran-2-onov z maleinanhidridom, pri katerih so glavni produkti različno substituirani biciklo[2.2.2]okteni, v nekaterih primerih pa je možen tudi nastanek aromatskih derivatov izobenzofurana. Analiza rezultatov omogoča vpogled v vplive na reaktivnost 2H-piran-2-onov v Diels–Alderjevih reakcijah.
Keywords
heterociklična kemija;2H-piran-2-oni;biciklo[2.2.2]okteni;Diels-Alderjeva reakcija;magistrska dela;
Data
Language: |
Slovenian |
Year of publishing: |
2023 |
Typology: |
2.09 - Master's Thesis |
Organization: |
UL FKKT - Faculty of Chemistry and Chemical Technology |
Publisher: |
[K. B. Reberc] |
UDC: |
547.81(043.2) |
COBISS: |
173236227
|
Views: |
87 |
Downloads: |
17 |
Average score: |
0 (0 votes) |
Metadata: |
|
Other data
Secondary language: |
English |
Secondary title: |
Synthesis and derivatization of novel 3-benzoylamino-2H-pyran-2-ones to bicyclo[2.2.2]octene compounds |
Secondary abstract: |
The master's thesis presents 2H-pyran-2-ones, different synthetic routes and their reactivity in various reactions. One of the possible transformations is via cycloaddition reactions leading to interesting bicyclo[2.2.2]octene systems. In the experimental work, I focused on the reactions of 2H-pyran-2-ones with maleic anhydride, in which the main products are variously substituted bicyclo[2.2.2]octenes, with possible formation of aromatic derivatives of isobenzofuran in some cases. Analysis of the results provides insight into the effects on the reactivity of 2H-pyran-2-ones in Diels–Alder reactions. |
Secondary keywords: |
2H-pyran-2-ones;bicyclo[2.2.2]octenes;heterocyclic chemistry;Diels-Alder reaction;Pirani;Organska sinteza (kemija);Univerzitetna in visokošolska dela; |
Type (COBISS): |
Master's thesis/paper |
Study programme: |
1000375 |
Embargo end date (OpenAIRE): |
1970-01-01 |
Thesis comment: |
Univ. v Ljubljani, Fak. za kemijo in kemijsko tehnologijo, smer Kemija |
Pages: |
66 str. |
ID: |
19999899 |