| Course label : | Carbohydrate chemistry |
|---|---|
| Teaching departement : | CMA / |
| Teaching manager : | Mister CHRISTEL PIERLOT |
| Education language : | |
| Potential ects : | 0 |
| Results grid : | |
| Code and label (hp) : | ENSCL_CI_M8_B3_3_SUPP - Chimie des sucres |
Education team
Teachers : Mister CHRISTEL PIERLOT / Mister RAPHAEL LEBEUF / Mister VANGELIS AGOURIDAS
External contributors (business, research, secondary education): various temporary teachers
Summary
After a short remind on photosynthesis and energy storage, the structural aspect of saccharides (mono, di, poly) is discussed. We then approach notions of stability (oxidation, reduction, acid/base, thermical). In a third part, the use of monosaccharides as a molecular brick is addressed in the synthesis of synthetic molecules of biological interest.
Educational goals
Have a vision of set on the carbohydrate structure (mono, di et polysaccharides) and their use as agro sourced building blocks in the synthesis of biological active molecules Be able to apply the protection/deprotection strategy to the carbohydrate chemistry and design synthesis of mono and disaccharides of biological interest (ex : 18-fluoroglucose for positron emission tomography, Tamiflu, AZT)
Sustainable development goals
Knowledge control procedures
Continuous Assessment
Comments: Written test (1h), questions on the curse and exercises
Online resources
Pedagogy
Power point course and manuscript
Sequencing / learning methods
| Number of hours - Lectures : | 5 |
|---|---|
| Number of hours - Tutorial : | 3 |
| Number of hours - Practical work : | 0 |
| Number of hours - Seminar : | 0 |
| Number of hours - Half-group seminar : | 0 |
| Number of student hours in TEA (Autonomous learning) : | 0 |
| Number of student hours in TNE (Non-supervised activities) : | 0 |
| Number of hours in CB (Fixed exams) : | 0 |
| Number of student hours in PER (Personal work) : | 0 |
| Number of hours - Projects : | 0 |
Prerequisites
Organic chemistry L3 level : chemistry of carbonyl group (acetalisation), reactivity, oxidation and protection/deprotection of the OH functions (alcohol and acetal) as well as stereochemistry and conformational equilibrium notions, RMN.