Related Experiment Video
Updated: May 1, 2026

Rapid One-step Enzymatic Synthesis and All-aqueous Purification of Trehalose Analogues
Published on: February 17, 2017
Bio-inspired synthesis of rare and unnatural carbohydrates and cyclitols through strain driven epimerization
Raja Mohanrao1, Aromal Asokan, Kana M Sureshan
1School of Chemistry, Indian Institute of Science Education and Research, Thiruvananthapuram, CET-Campus, Thiruvananthapuram-695016, India. kms@iisertvm.ac.in.
Abstract:
We report a bio-inspired, strain driven epimerization of trans-ketals to cis-ketals through an enolate intermediate. Swern oxidation of a hydroxyl group adjacent to a trans-ketal effects both oxidation and its epimerization to cis-ketal. This novel and general strategy allows inversion of up to three contiguous stereocenters and has been illustrated by the synthesis of several unnatural/rare isomers of carbohydrates/cyclitols from their naturally abundant isomers.
Related Concept Videos
Bioreactor Controls-III
Biosynthesis of Polysaccharides
Synthetic Biology
Golden rice
Golden rice is a genetically modified...
Cycloaddition Reactions: Overview
ATP and Macromolecule Synthesis
Most macromolecules are composed of single subunits, or building blocks, called monomers. The monomers combine with each other using covalent bonds to form larger molecules known as polymers.
Conversion of...
Biosynthesis in Bacteria

