Related Experiment Video
Updated: Sep 19, 2025

Preparation of Stable Bicyclic Aziridinium Ions and Their Ring-Opening for the Synthesis of Azaheterocycles
Published on: August 22, 2018
Ag(I)-Catalyzed C-C Bond Cleavage and Re-Assembly Reactions Between 2H-Azirines and α-Carbonyl Sulfoxonium Ylides
Yiding Wang1, Yan Wang2, Yangu Liu1
1College of Science, Sichuan Agricultural University, Ya'an, Sichuan 625014, China.
Abstract:
In this report, we describe the Ag(I)-N,N'-dioxide complex-catalyzed C-C bond cleavage and reassembly reactions between 2H-azirines and α-carbonyl sulfoxonium ylides, leading to an unusual formal insertion of enamine into unstrained C-C bonds. This procedure provides rapid access to a series of otherwise inaccessible α,β-unsaturated imines. Detailed mechanistic studies reveal that this catalytic transformation proceeds through a tandem sequence involving a radical-mediated formal [3 + 2] cycloaddition reaction, C-C bond cleavage, and elimination processes.
More Related Videos
Related Concept Videos
Alkynes to Carboxylic Acids: Oxidative Cleavage
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Overview
Preparation of 1° Amines: Azide Synthesis
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...
Aldehydes and Ketones to Alkenes: Wittig Reaction Mechanism
The reaction begins with the nucleophilic addition between a phosphorus ylide and the carbonyl compound. Due to its carbanionic character, phosphorus ylide acts as a strong nucleophile and attacks the electrophilic carbonyl group. This generates a charge-separated dipolar intermediate called betaine. The negatively charged oxygen atom and...
Acid Halides to Esters: Alcoholysis

