Reactivity and regioselectivity in the ring opening of 2-substituted non-activated aziridines: A density functional theory based analysis
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference27 articles.
1. Rearrangement of β-amino alcohols via aziridiniums: a review;Métro;Chem. Soc. Rev.,2010
2. Regioselectivity in the ring opening of non-activated aziridines;Stanković;Chem. Soc. Rev.,2012
3. Systematic study of halide-induced ring opening of 2-substituted aziridinium salts and theoretical rationalization of the reaction pathways;D’hooghe;Eur. J. Org. Chem.,2010
4. Opposite regiospecific ring opening of 2-(cyanomethyl)aziridines by hydrogen bromide and benzyl bromide: experimental study and theoretical rationalization;Catak;J. Org. Chem.,2010
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2. (Salen)Mn(III)-Catalyzed Enantioselective Intramolecular Haloamination of Alkenes through Chiral Aziridinium Ion Ring-Opening Sequence;ACS Catalysis;2022-06-01
3. Nucleophilicity and CO2 fixation ability of phosphorus, nitrogen and sulfur ylides: insights on stereoelectronic factors from DFT study;Journal of Chemical Sciences;2021-11-24
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