Related Experiment Video
Updated: May 24, 2026

From a Natural Product to Its Biosynthetic Gene Cluster: A Demonstration Using Polyketomycin from Streptomyces diastatochromogenes Tü6028
Published on: January 13, 2017
[Study on semi-synthetic transforming technology for the natural product of isocorydione]
Tian-Cai Zhang1, He-Lin Ye, Jun-Xi Liu
1School of Pharmay, Gansu College of Traditional Chinese Medicine, Lanzhou 730000, China.
Abstract:
Transforming technology for semi-synthesized isocorydione from the natural product ofisocorydine was studied. The factors affecting on the reaction yield were investigated. UV spectrophotometry was used to indicate the semi-synthesized yield of isocorydione. The optimum reaction conditions were determined as following: reacting for 12 h in the solution of sodium dihydrogen phosphate at pH 10, the temperature was 25 degrees C and the ratio of isocorydine to Fremy's radical was 1 : 2. Under the optimum conditions, the yield could reach up to 50.0%. The molecular structure of isocorydione was elucidated by X-ray single-crystal diffraction analysis for the first time.
Related Concept Videos
Stereoisomerism of Cyclic Compounds
Production of Pharmaceuticals
Diels–Alder Reaction Forming Cyclic Products: Stereochemistry
Stereoisomers

![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)