An oxidative expansion mechanism of isatin-derived imines
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s12039-024-02283-5.pdf
Reference15 articles.
1. Singh G S and Desta Z Y 2012 Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks Chem. Rev. 112 6104. https://doi.org/10.1021/cr300135y
2. Davidovich P, Novikova D, Tribulovich V, Smirnov S, Gurzhiy V, Melino G and Garabadzhiu A 2014 First X-ray structural characterization of isatin. Schiff base derivative NMR and theoretical conformational studies J. Mol. Struct. 1075 450. https://doi.org/10.1016/j.molstruc.2014.07.008
3. Raman N, Sobha S and Mitu L 2012 Synthesis, structure elucidation, DNA interaction, biological evaluation, and molecular docking of an isatin-derived tyramine bidentate Schiff base and its metal complexes Monatsh. Chem. 143 1019. https://doi.org/10.1007/s00706-011-0699-8
4. Garden S J and Skakle J M 2002 Isatin derivatives are reactive electrophilic components for the Baylis-Hillman reaction Tetrahedron Lett. 43 1969. https://doi.org/10.1016/S0040-4039(02)00160-0
5. Sheng F T, Li Z M, Zhang Y Z, Sun L X, Zhang Y C, Tan W and Shi F 2020 Atroposelective synthesis of 3,3′-bisindoles bearing axial and central chirality: using isatin-derived imines as electrophiles Chinese J. Chem. 38 583. https://doi.org/10.1002/cjoc.202000022
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