Chemistry of polyvalent iodine. - Abstract - Europe PMC
Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide and unactivated C(sp3)–H bonds | Communications Chemistry
/8F1232C6EE59D103802585F90071D7DB/$file/FI10879_structure.png "Iodobenzene 1,1-diacetate | 3240-34-4 | Biosynth Carbosynth")
Iodobenzene 1,1-diacetate | 3240-34-4 | Biosynth Carbosynth
Iodobenzene - an overview | ScienceDirect Topics
Frontiers | Hypervalent Iodine Reagents in Palladium-Catalyzed Oxidative Cross-Coupling Reactions | Chemistry
Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC Publishing) DOI:10.1039/C7RA11875A
Carbonyl oxidation with hypervalent iodine reagents - Wikipedia
JVWU, Oxidation with iodo benzene di acetate , M.Sc chemistry 2 year - YouTube
Zeolite Encapsulated Fe-poprhyrin for Catalytic Oxidation with Iodobenzene Diacetate (PhI(OAc)2)
Recent Advances in Iodosobenzene‐Mediated Construction of Heterocyclic Scaffolds: Transition‐Metal‐Free Approaches and Scope - Gayen - 2018 - European Journal of Organic Chemistry - Wiley Online Library
Iodosobenzene Diacetate
![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 ...
Carbonyl oxidation with hypervalent iodine reagents - Wikipedia
TEMPO Oxidation | Chem-Station Int. Ed.
organic chemistry - Mechanism of oxidative dearomatisation with hypervalent iodine - Chemistry Stack Exchange
Iodosobenzene Diacetate
Scheme 2 Proposed mechanism for the oxidation of 2 to 3. | Download Scientific Diagram
Supplemental Topics
Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC Publishing) DOI:10.1039/C7RA11875A
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
Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide and unactivated C(sp3)–H bonds | Communications Chemistry
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
Iodobenzene diacetate (IBD) catalyzed an quick oxidative aromatization of Hantzsch-1,4-dihydropyridines to pyridines under ultrasonic irradiation - ScienceDirect
PDF) Hypervalent iodine(III)-mediated oxidation of aldoximes to N-acetoxy or N-hydroxy amides
