Factors influencing the reverse-Cope approach to 1,2,5-oxadiazinanes from allylamines and nitrones: Optimization of a new vicinal diamine synthesis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Retro-Cope eliminations in the synthesis of 1,2,5-oxadiazinanes from allylamines and nitrones: a method for the amination of unactivated alkenes
2. Cyclization of unsaturated hydroxylamine derivatives
3. Nitrones and oxaziridines. XXII. Preparation and cyclization of some δ,ε-unsaturated hydroxylamines
4. The regiochemistry of intramolecular n-alkenylnitrone additions: preparative and mechanistic implications
5. Suprafaciality of Thermal N-4-Alkenylhydroxylamine Cyclizations: syntheses of (.+-.)-.alpha.-Lycorane and (+)-Trianthine
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1. Strategies for Direct, Transition Metal‐Free Addition of Nitrogen Synthons to Alkenes;Helvetica Chimica Acta;2023-12-15
2. Synthesis of 1,2,5‐Oxadiazinane Derivatives by Photochemical Cycloaddition of Nitrones with Diaminomethanes;ChemPhotoChem;2020-02-25
3. Cobalt-Catalyzed Intermolecular Markovnikov Hydroamination of Nonactivated Olefins: N2-Selective Alkylation of Benzotriazole;Organic Letters;2020-01-03
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