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Modern principles of organic synthesis are taught with the focus on reduction and oxidation of organic compounds, introduction of halogenes, nitro, nitroso, sulfo groups, application of alkylation and acylation reactions for design of a broad range of organic componds, application of organometallic compounds, application of diazonium salts, and formation of alkenes and alkynes by elimination reactions. Modern methods of transformation of the carbonyl and carboxylic groups. Principles of protection in organic synthesis. A very good knowledge of subjects Organic chemistry I, Organic Chemistry II, and Mechanisms of Organic Reactions is required. To be admitted, students will have to pass successfuly an introductory test.
Last update: Kundrát Ondřej (24.01.2018)
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The students have to pass two tests during the semester. The exam is combined - the students have to pass both a test and an oral part. Last update: Kundrát Ondřej (15.02.2018)
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Obligatory:
Recommended:
Last update: Kundrát Ondřej (18.06.2024)
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1. Principles of protection in organic synthesis. Protection of OH, CO, NH2 and COOH. 2. Functional derivatives of carbonyl and carboxylic group. Acetals, nitrogen derivatives. Formation of functional derivatives of carboxylic acids. 3. Halogenation. Addition and substitution reactions. Substitution of halogenes, O- and N-derivatives. 4. Alkylation a acylation reactions. Nucleophilic substitution, nucleophilic and alkylation reagents, PTC-catalysis. 5. Alkylation of heteroatoms, alkylation of C-acids. Base catalyzed aldolisation reactions. The Wittig and related reactions. 6. Friedel-Crafts alkylation and acylation, halomethylation, formylation. 7. Formation of organometallic compounds. 8. Aplication of organometallic compounds. 9. Nitration and nitrosation. Application for the synthesis of nitro and nitroso compounds. Sulfonation of aliphatic and aromatic compounds. 10. Formation and reactivity of diazonium salts. Diazotation, substitution of the diazo group, coupling reactions. 11. Elimination reactions. Mechanisms, dehydration, deoxygenations, elimination of N-, S-groups, halogenes, decarboxylation, extrusion. 12. Reduction. Catalytic hydrogenation, reduction of multiple bonds. 13. Reduction of functional groups, hydrogenolytic reactions. 14. Oxidation of a non-functional and functional carbon atom, hydroxylation, oxidation leading to carbonyl compounds and carboxylic acids. Oxidation of O, N, and S-functional groups, oxidative decarboxylation. Last update: Kundrát Ondřej (25.11.2021)
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No requirements for the students entering the UCT Prague for their whole Master or Double Master degree.
A mandatory entry tests for the students visiting the UCT Prague as Erasmus students a like. More details and a specimen entry test can be found at https://uoch.vscht.cz/studying/msc-subjects/orgsyn Last update: Kundrát Ondřej (26.11.2021)
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Teaching methods | ||||
Activity | Credits | Hours | ||
Účast na přednáškách | 1.5 | 42 | ||
Příprava na přednášky, semináře, laboratoře, exkurzi nebo praxi | 2.5 | 70 | ||
Příprava na zkoušku a její absolvování | 2 | 56 | ||
Účast na seminářích | 1 | 28 | ||
7 / 7 | 196 / 196 |