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Related Experiment Video

Updated: Feb 5, 2026

Electrochemically and Bioelectrochemically Induced Ammonium Recovery

Electrochemically and Bioelectrochemically Induced Ammonium Recovery

Published on: January 22, 2015

Ammonium Ylide Mediated Cyclization Reactions.

Lukas Roiser¹, Katharina Zielke¹, Mario Waser¹

¹Institute of Organic Chemistry, Johannes Kepler University Linz Altenbergerstr. 69 4040 Linz (Austria).

Asian Journal of Organic Chemistry

|September 14, 2018

Summary

This summary is machine-generated.

Ammonium ylides are increasingly used for asymmetric cyclization reactions, offering new synthetic routes. This review explores their potential and current limitations in chemical synthesis.

Keywords:

asymmetric synthesis cyclization heterocycles small ring systems ylides

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Area of Science:

Organic Chemistry
Asymmetric Synthesis

Background:

Ammonium ylides have gained prominence in organic synthesis over the last 20 years.
Cyclization reactions are crucial for constructing complex molecular architectures.

Purpose of the Study:

To introduce the field of ammonium ylide mediated cyclization reactions.
To highlight the potential and limitations of these methods in asymmetric synthesis.

Main Methods:

Review of recent literature on enantioselective protocols.
Focus on S-ylide-mediated strategies as a comparison.

Main Results:

Development of highly enantioselective protocols for annulation reactions.
Emergence of ammonium ylides as effective alternatives to other methods.

Conclusions:

Ammonium ylides show significant potential for asymmetric cyclization.
Further research is needed to overcome existing limitations and challenges.