Course: Special Seminar 4

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Course title Special Seminar 4
Course code OCH/OSE4
Organizational form of instruction Seminary
Level of course Master
Year of study not specified
Semester Summer
Number of ECTS credits 1
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. Oseltamivir (Corey), Oseltamivir (Fukuyama), Oseltamivir (Trost) 2. Reserpine (Stroke), Reserpine (Woodward) Strychine (Overman) 3. Strychine (MacMillan) Strychine (Mori) Strychine (Woodward), the design of drugs: inhibitors of kinases 4.Suaveoline, Tacamonine, Tirandamycin B; design the structure of drugs: Alzheimer's disease 5. Trifarienol B, U-106305, Virantmycin, design the structure of drugs: inhibitors of kinases 6. Wodeshiol, Yohimbine, Zaragozic acid, design the structure of drugs: inhibitors of metalloproteinases 7. Ziziphine, custom design and synthesis of natural substances 8. Custom design and synthesis of natural substances (3) 9. Custom design and synthesis of natural substances (3)

Learning activities and teaching methods
Dialogic Lecture (Discussion, Dialog, Brainstorming)
Learning outcomes
The seminar is designed to gain practical experience in synthetic procedures used in more complex organic molecules.
Ability to design a complete synthesis of chemical compounds.
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: Summer