Related Experiment Video
Updated: Feb 15, 2026

A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products
Published on: September 9, 2016
[Stereocontrolled Total Synthesis of Biologically Active Natural Products]
1Graduate School of Biomedical Sciences, Nagasaki University.
Abstract:
This review article describes the total syntheses of englerin A, ophiodilactones A and B, marinomycin A, N-methylwelwitindolinone C isothiocyanate, tirandamycins A-D, and tirandalydigin, which possess intriguing biological activities and challenging structures with characteristic ring systems. The focus is on the synthetic methodologies that lead to the highly stereocontrolled assembly of these natural products.
More Related Videos
07:59A High-Yield Streptomyces Transcription-Translation Toolkit for Synthetic Biology and Natural Product Applications
Published on: September 10, 2021
10:24A Fluorescence-based Protocol for Preliminary Screening of Protein Synthesis Inhibitors from Natural Sources
Published on: January 27, 2026
Related Concept Videos
What is Conservation Biology?
Drug Products: Biologics, Biosimilars and Interchangeables
Synthesis and Decomposition Reactions
What is Natural Selection?
Nature and Nurture
Biological Effects of Radiation