Related Experiment Video
Updated: Feb 14, 2026

Preparation and Use of Carbonyl-decorated Carbenes in the Activation of White Phosphorus
Published on: October 3, 2014
Modular Access to Azepines by Directed Carbonylative C-C Bond Activation of Aminocyclopropanes
1School of Chemistry, University of Bristol , Bristol, BS8 1TS, United Kingdom.
Abstract:
A modular Rh-catalyzed entry to azepines is outlined. Under a CO atmosphere, protecting group directed C-C bond activation of aminocyclopropanes provides rhodacyclopentanones. These intermediates are effective for intramolecular C-H metalation of either an N-aryl or N-vinyl unit en route to azepine ring systems. Thus, byproduct-free heterocyclizations are enabled by sequential C-C activation and C-H functionalization steps.
Related Concept Videos
Peptide Bonds
Bond Energies and Bond Lengths
IR Spectrum Peak Intensity: Amount of IR-Active Bonds
Bonding in Metals
Ionic Bonds
When atoms gain or lose electrons to achieve a more stable electron configuration they form ions. Ionic bonds are electrostatic attractions between ions with opposite charges. Ionic compounds are rigid and brittle when solid and may dissociate into their constituent ions in water. Covalent compounds, by contrast, remain intact unless a chemical reaction breaks them.
Opposing Charges Hold Ions Together in Ionic Compounds
Ionic bonds are reversible electrostatic interactions between ions...
Bond Dissociation Energy and Activation Energy

