Related Experiment Video
Updated: Jul 14, 2026

Single-step Purification of Macromolecular Complexes Using RNA Attached to Biotin and a Photo-cleavable Linker
Published on: January 3, 2019
A rapid synthesis of the biotin core through a tandem Michael reaction
1Department of Chemistry and Chemical Biology, Indiana University Purdue Univeristy Indianapolis, Indianapolis, Indiana 46202, USA. oh@chem.iupui.edu
Abstract:
A biotin core has been assembled in a short and efficient sequence utilizing a tandem intramolecular Michael reaction/fragmentation/Michael reaction from vinyl sulfoxide and sulfone alcohols (12 and 13).
Related Concept Videos
Conjugate Addition of Enolates: Michael Addition
Biosynthesis of Nucleic Acids
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
SN2 Reaction: Mechanism
The presence of the more electronegative halogen in the substrate creates a polarized carbon-halide bond. The halide pulls the electron cloud generating an electrophilic center at the carbon atom. Thus, the carbon atom carries a partial positive charge while the halide has a...
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...
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation

