Aziridine–allylsilane-mediated synthesis of exocyclic γ-amino olefins and azabicyclo[x.y.1]-systems
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. The synthesis of γ-amino olefins. A novel intramolecular aziridine — allylsilane reaction
2. Aziridine−Allylsilane-Mediated Total Synthesis of (−)-Yohimbane
3. Synthesis of bicyclic proline analogs using a formal [3 + 2] intramolecular aziridine-allylsilane cycloaddition reaction
4. Synthesis of (−)-Aphanorphine Using Aryl Radical Cyclization
5. An Approach to the Skeleton of the Securinega Alkaloids. The Total Synthesis of (±)-Securinine
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2. Selective C3-Allylation and Formal [3 + 2]-Annulation of Spiro-Aziridine Oxindoles: Synthesis of 5′-Substituted Spiro[pyrrolidine-3,3′-oxindoles] and Coerulescine;The Journal of Organic Chemistry;2022-06-22
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5. Synthesis of tubuphenylalanine and epi-tubuphenylalanine via regioselective aziridine ring opening with carbon nucleophiles followed by hydroboration-oxidation of 1,1-substituted amino alkenes;Tetrahedron;2018-11
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