Level of Education
4-year college degree
ECTS
2 credits
Training Structure
College of Sciences
Description
This course provides a concise and systematic overview of all aspects of heterocyclic chemistry, from nomenclature to applications such as the mechanisms of action of medications, toxins, and drugs, as well as pigments, food colorings, and more…
Hourly Volumes*:
CM: 3:00 p.m.
TD: 5 hours
Objectives
Become familiar with the nomenclature of heterocyclic compounds and their synthesis.
Explore the conventional methods for synthesizing common nitrogen-, oxygen-, and sulfur-containing heterocycles.
Be able to propose synthetic routes for the synthesis of heterocyclic molecules.
Class Hours
- Heterocyclic Chemistry - LectureLecture3:00 p.m.
- Heterocyclic Chemistry - TutorialTutorials5 hours
Mandatory Prerequisites
Organic Chemistry, L3 Level
Knowledge Assessment
2-hour final written exam
Authorized documents: No
Non-graphical calculators allowed: yes
Internet access allowed: No
Course Outline
Class: 15 hours
The chemistry and retrosynthesis of each major family of heterocycles (pyridines, diazines, quinolines, pyrroles, indoles, furans, thiophenes, azoles, purines, and pteridines) are covered systematically. The areas of application for each family of heterocycles are illustrated through concrete examples (active ingredients, drugs, flavorings, pigments, etc.).
- Nomenclature of Heterocycles
- General Methods for the Synthesis of Rings with 3, 4, 5, and 6 Atoms
- Palladium-Catalyzed Reactions in Heterocyclic Chemistry
- Heterocycles containing more than two heteroatoms
TD:5H
The tutorials provide an opportunity to illustrate and apply the concepts covered in class through exercises on nomenclature, synthesis, retrosynthetic analysis, and the reactivity of aromatic heterocycles, with a primary focus on 5- and 6-membered rings.
Additional Information
Teaching staff:
Michael Smietana,
Michael.smietana@umontpellier.fr
Jean-Pierre Uttaro
Jean-pierre.uttaro@umontpellier.fr