Aryl Halides - Globe Thesis

Keyword [Aryl Halides] Result: 61 - 80 \| Page: 4 of 5
61.	The Research On The Reaction Of Ortho-Functionalized Aryl Halides To Construct Nitrogen Heterocycle
62.	Base Promoted New Radical Reactions
63.	Studies Of Palladium-Catalyzed C-H Arylation And Copper-Catalyzed Cyanation Of Aryl Halides Reactions In PEG-400
64.	Mechanistic Investigation Of Palladium-Catalyzed Amidation Of Aryl Halides
65.	Palladium-catalyzed Carbonylation Of Aryl Halides With Formic Acid As The Carbon Monoxide Source
66.	Study On Preparation Of Olefin Via Nickel-Catalyzed Reductive Coupling Of Aryl Halides With Vinyl Bromides
67.	Study On The Reaction Of Silicon-bridged Diyne With Alkynes And Aryl Halides Mediated By Zirconocene
68.	Nickel-catalyzed Reductive Coupling Of Unactivated Tertiary Alkyl Halides With Aryl Halides
69.	Visible-light Catalyzed Functionalization Of Aryl Halides And Amino Acid Derivatives
70.	Nickel-Catalyzed Reductive Cross-Coupling Of Trifluoroethyl Halides And Related Derivatives With(Hetero) Aryl Halides/Synthesis Of Polyethylene Glycol Macrocyclic Sulfate
71.	Visible-Light Enhanced Base-Promoted Dehalogenations And Carbonylative Cyclizations Involving Aryl Radicals
72.	Pd/Al(OH)3 Nanopaticles-catalyzed Stille Cross-coupling Reactions Of Aryl Halides
73.	A Palladium Nanoparticles Catalyst For The Suzuki Cross-coupling Reactions Of Aryl Halides And Potassium Aryltrifluoroborates
74.	Nickel-Catalyzed Aminocarbonylation Of Aryl Halides Using Carbamoylsilane As An Amide Source
75.	Nickel-Catalyzed Reductive Cross-coupling Of(Hetero) Aryl Halides With Mono-/Di-fluoromethyl Halides
76.	Ionic And Neutral Phosphines:Synthesis, Characterization And Application To Carbonylations
77.	A Novel Method For The Synthesis Of Triarylphosphines Under Transition-Metal-Free Conditions
78.	The Novel Cyanation Reactions With Formamide As Cyanide Source
79.	Synthesis And Photocatalytic Properties Of Bay-Substituted Perylene Diimide Derivatives
80.	Intramolecular Nucleophilic Addition Of Aryl-halides To ?-ketoamides And ?-iminoamides:Synthetic Access To Oxindole
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