Related Experiment Video
Updated: Nov 17, 2025

Improved In-gel Reductive β-Elimination for Comprehensive O-linked and Sulfo-glycomics by Mass Spectrometry
Published on: November 20, 2014
Total Synthesis and Structure Revision of a Fungal Glycolipid Fusaroside
Santanu Jana1, Vikram A Sarpe1, Suvarn S Kulkarni1
1Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India.
Abstract:
Herein, we report a strategy for the total synthesis of a structurally unique fungal glycolipid fusaroside. The first total synthesis of the proposed structure involved construction of the complex, branched lipid chain having a variety of alkenes with E stereochemistry and attachment of the masked α,β-unsaturated β-keto acid at the O-4 position of trehalose as key steps. We propose a revision in the structure of fusaroside, particularly the position of olefins in the lipid chain.
Related Concept Videos
Formation of Lipopolysaccharides
Oligosaccharide Assembly
Multiple sugar molecules that may or may...
Biosynthesis of Lipids
Biosynthesis of Polysaccharides
Peptidoglycan Synthesis
Structure of Lipids

