An unexpected di-amination between isatin N,N′-cyclic azomethine imine 1,3-dipole and azodicarboxylates via C3 umpolung of oxindole
Author:
Funder
National Key Research and Development Program of China
Publisher
Elsevier BV
Reference22 articles.
1. Efficient Asymmetric Synthesis of Novel Gastrin Receptor Antagonist AG-041R via Highly Stereoselective Alkylation of Oxindole Enolates
2. Design and synthesis of novel HIV-1 protease inhibitors incorporating oxyindoles as the -ligands
3. Synthesis and biological evaluation of 3-amino-3-hydroxymethyloxindoles as potential anti-cancer agents
4. Asymmetric organocatalytic N-nitroso-aldol reaction of oxindoles
5. Organocatalytic asymmetric allylic amination of Morita–Baylis–Hillman carbonates of isatins
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1. A novel [4 + 3] annulation between isatin N,N’-cyclic azomethine 1,3-dipole and in situ generated nitrosoalkene for direct preparation of seven-membered heterocyclic spirooxindoles;Tetrahedron Letters;2024-08
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