Synthesis of quaternary allylammonium salts via ring opening of 1-benzyl-2-(bromomethyl)aziridines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Electron transfer induced ring opening of 2-(bromomethyl)aziridines by magnesium in methanol
2. Radical-Induced Ring Opening of 2-(Bromomethyl)aziridines
3. Regiospecific Reductive Cleavage of the C(2)−N Bond of Aziridines Substituted with an Electron Acceptor Mediated by Mg/MeOH
4. Sonochemical cleavage of 2-(bromomethyl)aziridines by a zinc–copper couple
5. Synthesis of pyrrolizidines by cascade reactions of N-alkenylaziridinylmethyl radicals
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1. Synthesis of Alkyl 3-Chloroazetidine-3-carboxylates via Regioselective Ring Transformation of Alkyl 2-(Bromomethyl)aziridine-2-carboxylates;HETEROCYCLES;2014
2. An efficient procedure for the synthesis of phenacyl and benzyl azolium salts using fluorous alcohols;Journal of the Iranian Chemical Society;2013-12-06
3. Synthesis of 3-Methoxyazetidines via an Aziridine to Azetidine Rearrangement and Theoretical Rationalization of the Reaction Mechanism;The Journal of Organic Chemistry;2011-03-09
4. Microwave-assisted regioselective ring opening of non-activated aziridines by lithium aluminium hydride;Organic & Biomolecular Chemistry;2010
5. First tandem nucleophilic addition–electrophilic amination reaction of Eschenmoser’s salts: synthesis of cyclic and spiro-fused hydrazonium salts;Tetrahedron Letters;2007-10
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