Ti-Catalyzed and -Mediated Oxidative Amination Reactions

Keyphrases

• Acceptor Substrate 11%
• Alkenes 22%
• Alkynes 100%
• Aminated 11%
• Amination 100%
• Amination Method 22%
• Aryl 11%
• Azobenzene 11%
• Back-donation 11%
• Carboamination 11%
• Catalytic Applications 11%
• Catalytic Cycle 11%
• Catalytic Reaction 11%
• Catalytic Redox 11%
• Catalytic Turnover 11%
• Component Mode Synthesis 11%
• Condensation 11%
• Cycloaddition 11%
• Cyclopropylimine 11%
• Diazene 11%
• Direct Bond 11%
• Early Transition Metal 22%
• Earth-abundant 11%
• Electrocyclic Reactions 11%
• Electron-rich 11%
• Elimination Method 11%
• Functional Groups 11%
• Heteroaromatics 11%
• Heterocycle Synthesis 11%
• Heterocycles 11%
• High-valent 11%
• Imination 11%
• Isocyanide 11%
• Late Transition Metal 11%
• Low-valent 11%
• Mechanistic Studies 22%
• Mechanistic Understanding 11%
• Multicomponent Coupling Reactions 11%
• Nitriles 22%
• Organic Azides 11%
• Oxidative Amination 100%
• Oxidative Coupling 22%
• Pericyclic Reactions 11%
• Pyrazole 11%
• Pyrrole 11%
• Pyrrole Synthesis 11%
• Reaction Development 11%
• Reaction Mechanism 11%
• Reactive Small Molecules 11%
• Reactive Species 11%
• Reactivity Pattern 11%
• Redox 11%
• Redox Catalysis 11%
• Redox Non-innocent 11%
• Redox Processes 11%
• Reductive Elimination 11%
• Ring Opening 11%
• Rutile 11%
• Strained Alkenes 11%
• Substitution Pattern 11%
• Ti(IV) 22%
• α,β-unsaturated Imines 11%

Chemistry

• Alkene 33%
• Alkyne 100%
• amination 100%
• Azide 11%
• Azobenzene 11%
• catalytic cycle 11%
• Catalytic Reaction 11%
• Condensation 11%
• Coupling Reaction 11%
• Cycloaddition 11%
• Diazene 11%
• Heterocyclic Compound 22%
• imination 11%
• Imine 11%
• Isocyanide 11%
• Mechanistic Study 22%
• Nitrile 22%
• Pericyclic Reaction 11%
• Pyrazole 11%
• Pyrrole 11%
• Redox Catalysis 11%
• Redox Process 11%
• Redox Reactions 11%
• Reductive Elimination Reaction 11%
• Ring Opening Reaction 11%
• stability 11%
• Titanium 11%
• Transition Metal 33%