Stereochemistry Course
This course delivers comprehensive mastery of stereochemistry, encompassing R/S designation, projection methods, isomer distinctions, analytical techniques, and the pivotal role of chirality in pharmaceutical activity. It equips learners with enhanced analytical prowess for research endeavours, process optimisation, and compliance-focused documentation in scientific and industrial settings.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
Gain expertise in three-dimensional molecular structures and accurately determine R/S configurations through this specialised Stereochemistry course. Participants will engage with wedge-dash, Fischer, and Newman projections, investigate enantiomers, diastereomers, and meso compounds, and understand chirality's influence on biological functions. Acquire effective techniques for synthesising single enantiomers, precise analytical approaches, and professional reporting aligned with contemporary research and regulatory standards.
Elevify advantages
Develop skills
- Develop proficiency in 3D stereochemical depictions including wedge-dash, Fischer, and Newman projections.
- Swiftly assign R/S configurations via Cahn-Ingold-Prelog rules, sidestepping frequent assessment errors.
- Evaluate chiral pharmaceuticals by associating enantiomers with receptor interactions, metabolic pathways, and toxicological profiles.
- Plan syntheses of individual enantiomers employing resolution, chiral auxiliaries, and catalytic strategies.
- Articulate stereochemical details effectively through IUPAC nomenclature, SMILES notation, NMR spectra, and HPLC analyses.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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