Catalysts | Free Full-Text | Recent Advances in Homogeneous Metal-Catalyzed Aerobic C–H Oxidation of Benzylic Compounds | HTML
The reaction of terminal alkynes with PhI(OAc)2: a convenient procedure for the preparation of α-acyloxy ketones - ScienceDirect
Hypervalent iodine reagents for heterocycle synthesis and functionaliz | ROC
Carbonyl oxidation with hypervalent iodine reagents - Wikipedia
Molecules | Free Full-Text | Hypervalent Iodine Reagents in High Valent Transition Metal Chemistry | HTML
Zeolite Encapsulated Fe-poprhyrin for Catalytic Oxidation with Iodobenzene Diacetate (PhI(OAc)2)
PDF) Nitrate as a Redox Co-Catalyst for the Aerobic Pd-Catalyzed Oxidation of Unactivated sp(3)-C-H Bonds
PhI(OAc)2-mediated functionalisation of unactivated alkenes for the synthesis of pyrazoline and isoxazoline derivatives - Organic & Biomolecular Chemistry (RSC Publishing)
Scheme 5 Plausible reaction mechanism & control experiments. | Download Scientific Diagram
Benoît Moreau Organohypervalent Iodine as Mild and Selective Reagents for Multiple Oxidation Processes Literature Meeting June 6 th, ppt download
Practical application of PhI(OAc)2/I2 combination to synthesize benzimidazoles from 2-aminobenzylamine through ring distortion strategy - ScienceDirect
Copper‐Catalyzed Decarboxylative Methylation of Aromatic Carboxylic Acids with PhI(OAc)2 - Jiang - 2014 - European Journal of Organic Chemistry - Wiley Online Library
Catalytic hypervalent iodine oxidation of alcohols to corresponding aldehydes or ketones using 2,2,6,6-tetramethylpiperidinyl-1-oxy and potassium peroxodisulfate | SpringerLink
PPT - Benoît Moreau PowerPoint Presentation, free download - ID:2778505
Metal-free mild oxidation of 5-hydroxymethylfurfural to 2,5-diformylfuran
Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III) reagents: an opportunity for rational catalyst design? - ScienceDirect
Phenol oxidation with hypervalent iodine reagents - Wikipedia
Copper-Promoted Functionalization of Organic Molecules: from Biologically Relevant Cu/O2 Model Systems to Organometallic Transformations. - Abstract - Europe PMC
TEMPO Oxidation | Chem-Station Int. Ed.
Frontiers | Hypervalent Iodine-Mediated Diastereoselective α-Acetoxylation of Cyclic Ketones | Chemistry
A highly efficient TEMPO mediated oxidation of sugar primary alcohols into uronic acids using 1-chloro-1,2-benziodoxol-3(1H)-one at room temperature - ScienceDirect
TEMPO
Hypervalent iodine reagents for heterocycle synthesis and functionaliz | ROC
Carbonyl oxidation with hypervalent iodine reagents - Wikipedia
Zeolite Encapsulated Fe-poprhyrin for Catalytic Oxidation with Iodobenzene Diacetate (PhI(OAc)2)
TEMPO Oxidation | Chem-Station Int. Ed.
