Course: Special Seminar 3

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Course title Special Seminar 3
Course code OCH/OSE3
Organizational form of instruction Seminar
Level of course Master
Year of study not specified
Semester Winter
Number of ECTS credits 2
Language of instruction Czech
Status of course Compulsory
Form of instruction Face-to-face
Work placements This is not an internship
Recommended optional programme components None
Lecturer(s)
  • Cankař Petr, doc. RNDr. Ph.D.
Course content
Students will work up total synthesis according to the article which is subsequently presented to the next lesson, ideally in PowerPoint or after conversion to PDF. The content presentation is the introduction of the audience with the particular compound, the retro-synthetic analysis and description of the whole synthesis, including reagents, yieldsand so on. The student must demonstrate that it has the synthesis, or the publication well-rehearsed, as he can expect questions from other students and the teacher. For each synthesis are enclosed tasks that need to be resolved and think about them. The successful solution of tasks need to be done other literature search, or use the attached article and references cited therein, alternatively consult with other students or the teacher. Tasks and solutions must be part of the presentation.All reaction schemes used in the presentation is necessary to paint in ChemDraw or ACD ChemSketch (alternatively another drawing program) and apply formatting ACS Style. Copy schemes from other sources is unacceptable. Processed themes (synthesis): 1.Aflatoxin B1 (Trost) Aflatoxin B1 (Büchi), Aflatoxin B2 2.Alkaloid 251F, Alstonerine, Aplysina 3.Capnellene, Dibromophakellstatin (Romo) Dibromophakellstatin (Austin) 4. Epibatidine (Evans) Epibatidine (Aggarwal) Epibatidine (Armstrong) 5. Indolizine 223A (Davis) indolizine 223A (MA) Acromelobinic Acid 6. Luciduline (Oppolzer) Luciduline (Evans) 7. Lysergic Acid, Grandisin D, Epibatidine (Regan) 8. Bikaverin, Fuchsiaefolin, Marinopyrol B 9. Dysibetain, Magallanesine, Mersicarpin 10. Mycophenolic acid, Nufaramin, Oseltamivir 11. Pancracine, Marasmic acid., Mesembrin 12. Final task - to custom design the synthesis of natural substance

Learning activities and teaching methods
Dialogic Lecture (Discussion, Dialog, Brainstorming)
Learning outcomes
The course is established to improve communication and orientation in chemical scientific literature.
Integrate knowledge, propose solutions, formulate conclusions
Prerequisites
unspecified

Assessment methods and criteria
Student performance

100% attendance. Including the presentation of tasks to level. Active involvement in discussions on other students' presentations.
Recommended literature
  • According to the chosen theme..
  • Dle zvoleného tématu..


Study plans that include the course
Faculty Study plan (Version) Category of Branch/Specialization Recommended year of study Recommended semester
Faculty: Faculty of Science Study plan (Version): Bioorganic Chemistry and Chemical Biology (2020) Category: Chemistry courses 2 Recommended year of study:2, Recommended semester: Winter