Regioselectivity in the ring opening of non-activated aziridines - Chemical Society Reviews (RSC Publishing)
Aziridines - Wikipedia
Aziridine Ring Opening: An Overview of Sustainable Methods - Sabir - 2018 - ChemistrySelect - Wiley Online Library
A Stepwise Synthesis of Spiroindoline Compounds via Ring Opening of Aziridines and C−H Activation/Cyclization - Xing - 2021 - Advanced Synthesis & Catalysis - Wiley Online Library
Aziridine ring opening and 2+3 cycloaddition reaction - YouTube
Transformations of aziridines to N-heterocycles. a Typical transition... | Download Scientific Diagram
File:Aziridine.svg - Wikimedia Commons
Nucleophilic ring opening reactions of aziridines | SpringerLink
Scheme 3. Regioselective ring-opening reactions of the [3.1.0] bicyclic... | Download Scientific Diagram
Aziridines - Wikipedia
Regioselectivity in the ring opening of non-activated aziridines - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C1CS15140A
![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")
Intermolecular [3+3] ring expansion of aziridines to dehydropiperi-dines through the intermediacy of aziridinium ylides | Nature Communications
Scheme 76 | Nucleophilic ring opening reactions of aziridines | SpringerLink
Nucleophilic ring opening reactions of aziridines | SpringerLink
Molecules | Free Full-Text | Alkylative Aziridine Ring-Opening Reactions | HTML
Aziridines and azetidines: building blocks for polyamines by anionic and cationic ring-opening polymerization - Polymer Chemistry (RSC Publishing) DOI:10.1039/C9PY00278B
Downstream Functionalization by Aziridine Ring Opening - Peptidomimetics II
File:Aziridine ring opening.svg - Wikipedia
Tandem aziridine ring opening-disulfide formation-reduction-Michael addition in one-pot mediated by tetrathiomolybdate - ScienceDirect
Enantioselective fluoride ring opening of aziridines enabled by cooperative Lewis acid catalysis - ScienceDirect
Aziridines - 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-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
