Related Experiment Video
Updated: Jun 7, 2025

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
Biomimetic Synthesis of the Marine-Derived Thioalkaloids Dassonmycins A and B
Tyler C Murgatroyd1, Tilo Söhnel1,2, Jonathan Sperry1
1School of Chemical Sciences, University of Auckland, 23 Symonds Street, Auckland, 1010, New Zealand.
Abstract:
A biomimetic synthesis of the marine thioalkaloids dassonmycins A and B is reported. The synthesis features a chemoselective reduction of a diketopiperazine to form a 2-piperazinone, which undergoes heteroannulation with naphthoquinone to yield dassonmycin A. Dassonmycin A undergoes slow cyclization to form dassonmycin B at physiological pH, supporting a biosynthesis hypothesis that this reaction could occur in the cytosol of the bacterial host species.
More Related Videos
09:10Synthesis of Masarimycin, a Small Molecule Inhibitor of Gram-Positive Bacterial Growth
Published on: January 7, 2022
09:08From a Natural Product to Its Biosynthetic Gene Cluster: A Demonstration Using Polyketomycin from Streptomyces diastatochromogenes Tü6028
Published on: January 13, 2017
Related Concept Videos
Biosynthesis in Bacteria
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Biosynthesis of Lipids
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Synthetic Biology
Golden rice
Golden rice is a genetically modified...