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Mehl Schwachsinnig Variable iodobenzene diacetate oxidation mechanism Gegen den Willen Zwei Grad Gesandtschaft

PDF) Hypervalent iodine(III)-mediated oxidation of aldoximes to N-acetoxy  or N-hydroxy amides
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
Full article: Unusual synthesis of azines and their oxidative degradation to carboxylic acid using iodobenzene diacetate

Hypervalent iodine reagents for heterocycle synthesis and functionaliz | ROC
Hypervalent iodine reagents for heterocycle synthesis and functionaliz | ROC

Hypervalent Iodine Compounds
Hypervalent Iodine Compounds

Phenol oxidation with hypervalent iodine reagents - Wikipedia
Phenol oxidation with hypervalent iodine reagents - Wikipedia

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
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

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
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

Organic Syntheses Procedure
Organic Syntheses Procedure

Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated  oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC  Publishing) DOI:10.1039/C7RA11875A
Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC Publishing) DOI:10.1039/C7RA11875A

PDF) ChemInform Abstract: Regiospecific Oxidation of Polycyclic Aromatic  Phenols to Quinones by Hypervalent Iodine Reagents
PDF) ChemInform Abstract: Regiospecific Oxidation of Polycyclic Aromatic Phenols to Quinones by Hypervalent Iodine Reagents

Frontiers | Hypervalent Iodine Reagents in Palladium-Catalyzed Oxidative  Cross-Coupling Reactions | Chemistry
Frontiers | Hypervalent Iodine Reagents in Palladium-Catalyzed Oxidative Cross-Coupling Reactions | Chemistry

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
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

organic chemistry - Mechanism of oxidative dearomatisation with hypervalent  iodine - Chemistry Stack Exchange
organic chemistry - Mechanism of oxidative dearomatisation with hypervalent iodine - Chemistry Stack Exchange

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 ...

Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated  oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC  Publishing) DOI:10.1039/C7RA11875A
Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC Publishing) DOI:10.1039/C7RA11875A

Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide  and unactivated C(sp3)–H bonds | Communications Chemistry
Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide and unactivated C(sp3)–H bonds | Communications Chemistry

Hypervalent iodine reagents for heterocycle synthesis and functionaliz | ROC
Hypervalent iodine reagents for heterocycle synthesis and functionaliz | ROC

Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide  and unactivated C(sp3)–H bonds | Communications Chemistry
Iodine(III) promotes cross-dehydrogenative coupling of N-hydroxyphthalimide and unactivated C(sp3)–H bonds | Communications Chemistry

TEMPO Oxidation | Chem-Station Int. Ed.
TEMPO Oxidation | Chem-Station Int. Ed.

Iodobenzene 1,1-diacetate | 3240-34-4 | Biosynth Carbosynth
Iodobenzene 1,1-diacetate | 3240-34-4 | Biosynth Carbosynth

Phenol oxidation with hypervalent iodine reagents - Wikipedia
Phenol oxidation with hypervalent iodine reagents - Wikipedia

Supplemental Topics
Supplemental Topics

Iodobenzene - an overview | ScienceDirect Topics
Iodobenzene - an overview | ScienceDirect Topics

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
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