Novel 2,2,6,6‐Tetramethylpiperidine 1‐Oxyl–Iodobenzene Hybrid Catalyst for Oxidation of Primary Alcohols to Carboxylic Acids - Yakura - 2011 - Advanced Synthesis & Catalysis - Wiley Online Library
Hypervalent Iodine Compounds
Diacetoxyiodo)benzene 98 3240-34-4
Iodosobenzene Diacetate
Frontiers | Hypervalent Iodine Reagents in Palladium-Catalyzed Oxidative Cross-Coupling Reactions | Chemistry
PDF) Hypervalent iodine(III)-mediated oxidation of aldoximes to N-acetoxy or N-hydroxy amides
Full article: Unusual synthesis of azines and their oxidative degradation to carboxylic acid using iodobenzene diacetate
Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide and unactivated C(sp3)–H bonds | Communications Chemistry
Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC Publishing) DOI:10.1039/C7RA11875A
Iodobenzene diacetate (IBD) catalyzed an quick oxidative aromatization of Hantzsch-1,4-dihydropyridines to pyridines under ultrasonic irradiation - ScienceDirect
Chemistry of polyvalent iodine. - Abstract - Europe PMC
Chemistry of polyvalent iodine. - Abstract - Europe PMC
PDF) ChemInform Abstract: Regiospecific Oxidation of Polycyclic Aromatic Phenols to Quinones by Hypervalent Iodine Reagents
Carbonyl oxidation with hypervalent iodine reagents - Wikipedia
Iodane - Wikiwand
Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide and unactivated C(sp3)–H bonds | Communications Chemistry
Organic Syntheses Procedure
Scheme 2 Proposed mechanism for the oxidation of 2 to 3. | Download Scientific Diagram
A one-pot oxidative decarboxylation–Friedel-Crafts reaction of acyclic α-amino acid derivatives activated by the combination of iodobenzene diacetate ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B815227F
Phenol oxidation with hypervalent iodine reagents - Wikipedia
![A facile iodine(III)-mediated synthesis of 3-(3-aryl-1-phenyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridines via oxidation of 2-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)-1-(pyridin-2-yl)hydrazines and their antimicrobial evaluations | Organic and ...](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2F2191-2858-1-1/MediaObjects/13588_2011_Article_1_Figa_HTML.gif "A facile iodine(III)-mediated synthesis of 3-(3-aryl-1-phenyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridines via oxidation of 2-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)-1-(pyridin-2-yl)hydrazines and their antimicrobial evaluations | Organic and ...")
A facile iodine(III)-mediated synthesis of 3-(3-aryl-1-phenyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridines via oxidation of 2-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)-1-(pyridin-2-yl)hydrazines and their antimicrobial evaluations | Organic and ...
Hypervalent iodine reagents for heterocycle synthesis and functionaliz | ROC
A one-pot oxidative decarboxylation–Friedel-Crafts reaction of acyclic α-amino acid derivatives activated by the combination of iodobenzene diacetate ... - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/B815227F
