Intramolecular radical trapping in “set” ring opening of N-enoyl aziridines. A new mechanistic probe and a new synthesis of pyrrolidones.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. Electron attachment to N-benzoylaziridines followed by C–N homolysis of the aziridine ring
2. Reactions with aziridines. 33. Arene hydrides. Part 1. Highly regioselective ring cleavage of N-acylaziridines by "anthracene hydride" (anion of 9,10-dihydroanthracene). Intermediacy of a carbonyl adduct. Influence of nitrogen inversion on the ring opening
3. Suppressing the cyclization of (1-methyl-5-hexenyl)sodium
4. Evidence for single electron transfer in metal-halogen exchange. The reaction of organolithium compounds with alkyl halides.
5. Arene hydrides. 3. Selective 1,4-reduction of chalcone with anthracene hydride via base-induced fragmentation of their Michael adduct
Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Benzylic Fragmentation (BFR), an Aromatic Analogue of E1cB Including a Homolytic Variant, as either Nucleofugal or Homolytic Path to Aryl Stabilized Carbanions or Ketyls, respectively;Journal für praktische Chemie;2000-06
2. Competition in the sodium iodide catalysed isomerisation of some aziridines;Tetrahedron Letters;1998-06
3. 3,3-Dialkyl- and 3-Alkyl-3-Benzyl-Substituted 2-Pyrrolidinones: A New Class of Anticonvulsant Agents;Journal of Medicinal Chemistry;1996-01-01
4. Volume 1 References;Comprehensive Heterocyclic Chemistry II;1996
5. Aziridines and Azirines: Monocyclic;Comprehensive Heterocyclic Chemistry II;1996
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