Synthesis of azole-linked <i>s</i>-triazine-isatin molecular architectures as nanoscale DNA-targeting agents: a combined spectroscopic and computational study. [PDF]
Nanoscale AdvMushtaq A, Nazia B, Naseer MM.
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Festkörperuntersuchungen von Isatin und ausgewählten Isatin-Derivaten
, 2018 openaire +1 more source
Ion-Pair Hydrogen Atom Transfer Catalysis Enables Cr-Catalyzed Allylation of Ketones Using Hydrocarbon Alkenes. [PDF]
Angew Chem Int Ed EnglArii S +4 more
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Recent developments in the organocatalytic asymmetric cycloaddition/annulation reactions involving indolylmethanols. [PDF]
RSC AdvPatel A, Harshit, Iype E, Kumar I.
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Microwave-Assisted Organic Syntheses in Deep Eutectic Solvents: A Win-Win Association for Sustainable Chemistry. [PDF]
ChemistryOpenDelaye PO, Salami C, Thiery E.
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Chemoenzymatic Diazo Synthesis Enabled by Enzymatic Halide Recycling with Vanadium-Dependent Haloperoxidases. [PDF]
J Am Chem SocSharma M +7 more
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A Review an Isatin, Isatin Derivatives and their Pharmacological Activity
Research Journal of Pharmacology and Pharmacodynamics, 2021Isatin or 1H-indole-2, 3-dione is an indole derivative. Isatin is an important class of heterocyclic compounds. Recently, heterocyclic compounds analogues and their derivatives have attracted strong interest in medicinal chemistry due to their biological and pharmacological properties. The structure have offered a high value of diversity that is proven
S. Janet Beula +3 more
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Alkylation of isatins with trichloroacetimidates
Organic & Biomolecular Chemistry, 2022N-Alkylation or O-alkylation of isatins can be achieved utilizing trichloroacetimidate electrophiles with the major product being controlled by solvent effects. These reactions provide access to N-alkyl isatins, versatile scaffolds which are often employed in synthesis.
Nilamber A. Mate +3 more
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Synthesis of Isatin Derivatives.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
E. G. Mesropyan +3 more
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Abstract Isatin does not show fluorescence or phosphorescence under any conditions. After excitation it undergoes rapid intersystem crossing to the triplet state (τ = 340 ns in deaerated benzene). This triplet state is capable of hydrogen abstraction, yielding a product analogous to pinacol, isatide.
G. Haucke, B. Seidel, A. Graness
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