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529-0241-01L 6 Credits
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Natural Product Synthesis

Naturstoffsynthese

Lecturers & Examiners: Prof. em. Dr. Hans Jürg Borschberg
VVZ CR n/a

Last Updated: 2026-02-05 14:55:03

Abstract

After an introductory overview on secondary metabolites the terms synthetic strategy and tactics will be illustrated. In addition, reaction mechanisms and aspects of dynamic stereochemistry will be discussed.

Objective

To get to know some important retrosynthetic concepts. Increase and improve the knowledge concerning synthetically important reactions, their mechanisms and stereochemical implications.

Content

1.1. General aspects of natural products and secondary metabolites 1.2. Biogenetic pathways towards secondary metabolites 2. Mannich-reaction and iminiumion-cyclisations as key strategies in alkaloid synthesis 3. Cycloadditions and electrocyclic reaction as synthetic strategies 4. Biomimetic strategies 5. Tandem reactions as key steps in natural product synthesis

Resources

Lecture Notes

Single sheets corresponding with the shown and discussed overheads will be handed out. The exercises are handed out one after the other, sheets with the proposed solutions at the appropriate time.

Literature

No specific book is required. A standard textbook on Organic Chemistry, like Streitwieser, Vollhard, Morrison-Boyd and so on may be helpful. For students with an above-average interest in the subject, the books cited above in the German version offer additional intellectual stimulus.

General Information

Language
German
Frequency
Yearly recurring

Examination

Type
session examination
Mode
written 60 minutes
Aids
Keine.

Course Components

Type Title Time & Place Hours
lecture with exercise Naturstoffsynthese
  • Thu 09:45-11:30 (HCI D 4)
  • Fri 11:45-12:30 (HCI D 6)
3 h weekly

Offered In