Related Experiment Video
Updated: May 18, 2026

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
The total synthesis of corallopyronin A and myxopyronin B
Andreas Rentsch1, Markus Kalesse
1Institut für Organische Chemie, Centre of Biomolecular Drug Research, Leibniz University Hannover, Germany.
Abstract:
Leading the way: the synthesis of natural products with new biological targets is one of the driving forces for the development of new antibiotics. The synthesis of the two secondary metabolites corallopyronin and myxopyronin have been achieved, which are prominent leads for the inhibition of bacterial RNA polymerase.
More Related Videos
10:41The Logic, Experimental Steps, and Potential of Heterologous Natural Product Biosynthesis Featuring the Complex Antibiotic Erythromycin A Produced Through E. coli
Published on: January 13, 2013
14:11Synthesis of pH Dependent Pyrazole, Imidazole, and Isoindolone Dipyrrinone Fluorophores using a Claisen-Schmidt Condensation Approach
Published on: June 10, 2021
Related Concept Videos
Biosynthesis in Bacteria
Biosynthesis of Lipids
Biosynthesis of Polysaccharides
Biosynthesis of Nucleic Acids
Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine Reaction
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation