![PDF] Recent applications of aziridine ring expansion reactions in heterocyclic synthesis | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e154a08385bc9b0b26216a1d8f7b25260b67df13/3-Figure1-1.png "PDF] Recent applications of aziridine ring expansion reactions in heterocyclic synthesis | Semantic Scholar")
PDF] Recent applications of aziridine ring expansion reactions in heterocyclic synthesis | Semantic Scholar
Regiochemistry in aziridine ring opening reactions. | Download Scientific Diagram
![N-methylative aziridine ring opening and the synthesis of (S)-3-methylamino-3-[(R)-pyrrolidin-3-yl]propanenitrile - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402017308839-sc1.jpg "N-methylative aziridine ring opening and the synthesis of (S)-3-methylamino-3-[(R)-pyrrolidin-3-yl]propanenitrile - ScienceDirect")
N-methylative aziridine ring opening and the synthesis of (S)-3-methylamino-3-[(R)-pyrrolidin-3-yl]propanenitrile - ScienceDirect
File:Aziridine ring opening.svg - Wikipedia
Aziridines - Wikipedia
![N-methylative aziridine ring opening and the synthesis of (S)-3-methylamino-3-[(R)-pyrrolidin-3-yl]propanenitrile - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402017308839-fx1.jpg "N-methylative aziridine ring opening and the synthesis of (S)-3-methylamino-3-[(R)-pyrrolidin-3-yl]propanenitrile - ScienceDirect")
N-methylative aziridine ring opening and the synthesis of (S)-3-methylamino-3-[(R)-pyrrolidin-3-yl]propanenitrile - ScienceDirect
Regioselectivity in the ring opening of non-activated aziridines - Chemical Society Reviews (RSC Publishing)
Aziridine Ring Opening: An Overview of Sustainable Methods - Sabir - 2018 - ChemistrySelect - Wiley Online Library
Stereoselective Syntheses of 4-Oxa Diaminopimelic Acid and Its Protected Derivatives via Aziridine Ring Opening | Organic Letters
One-Pot Acid-Catalyzed Ring-Opening/Cyclization/Oxidation of Aziridines with N-Tosylhydrazones: Access to 1,2,4-Triazines | Organic Letters
Ring-Opening Reactions of Nonactivated Aziridines Catalyzed by Tris(pentafluorophenyl)borane | The Journal of Organic Chemistry
Enantioselective fluoride ring opening of aziridines enabled by cooperative Lewis acid catalysis - ScienceDirect
A Mild and Efficient Method for the Syntheses and Regioselective Ring- Opening of Aziridines
Ring Opening of 1,1'-Sulfonyl Bis-Aziridines Derived from L-Amino Acids and DFT Study of the Affinity Toward Different Nucleophiles | Bentham Science
One-Pot Acid-Catalyzed Ring-Opening/Cyclization/Oxidation of Aziridines with N‑Tosylhydrazones: Access to 1,2,4-Triazines - ScienceDirect
Molecules | Free Full-Text | Alkylative Aziridine Ring-Opening Reactions
Datei:Aziridine opening.png – Wikipedia
N-Aminopyridinium reagents as traceless activating groups in the synthesis of N-Aryl aziridines | Nature Communications
Ring Opening of Aziridines by Pendant Silanols Allows for Stereospecific Preparations of 1'-Amino-Tetrahydrofurans | Organic Chemistry | ChemRxiv | Cambridge Open Engage
Modular, One-Pot, Sequential Aziridine Ring Opening-S(N)Ar Strategy to 7-, 10-, and 11-Membered Benzo-Fused Sultams. - Abstract - Europe PMC
Regioselective Ring‐Opening Nucleophilic Addition of Aziridines through Photoredox Catalyst - Sun - 2014 - Advanced Synthesis & Catalysis - Wiley Online Library
Nucleophilic ring opening reactions of aziridines | SpringerLink
Organo-catalytic synthesis of tetrahydropyridines via a domino ring opening/cyclization reaction of aziridines | SpringerLink
Aziridines and azetidines: building blocks for polyamines by anionic and cationic ring-opening polymerization
![PDF] Recent applications of aziridine ring expansion reactions in heterocyclic synthesis | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e154a08385bc9b0b26216a1d8f7b25260b67df13/10-Figure2-1.png "PDF] Recent applications of aziridine ring expansion reactions in heterocyclic synthesis | Semantic Scholar")
PDF] Recent applications of aziridine ring expansion reactions in heterocyclic synthesis | Semantic Scholar
![Intermolecular [3+3] ring expansion of aziridines to dehydropiperi-dines through the intermediacy of aziridinium ylides | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-020-15134-x/MediaObjects/41467_2020_15134_Fig1_HTML.png "Intermolecular [3+3] ring expansion of aziridines to dehydropiperi-dines through the intermediacy of aziridinium ylides | Nature Communications")