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PIDA/I2-Mediated α- and β-C(sp3)–H Bond Dual Functionalization of Tertiary  Amines | The Journal of Organic Chemistry
PIDA/I2-Mediated α- and β-C(sp3)–H Bond Dual Functionalization of Tertiary Amines | The Journal of Organic Chemistry

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

Frontiers | Hypervalent Iodine-Mediated Diastereoselective α-Acetoxylation  of Cyclic Ketones | Chemistry
Frontiers | Hypervalent Iodine-Mediated Diastereoselective α-Acetoxylation of Cyclic Ketones | Chemistry

Phenyliodine(III) Diacetate (PIDA) Mediated Synthesis of Aromatic Azo  Compounds through Oxidative Dehydrogenative Coupling of Anilines: Scope and  Mechanism - Monir - 2014 - European Journal of Organic Chemistry - Wiley  Online Library
Phenyliodine(III) Diacetate (PIDA) Mediated Synthesis of Aromatic Azo Compounds through Oxidative Dehydrogenative Coupling of Anilines: Scope and Mechanism - Monir - 2014 - European Journal of Organic Chemistry - Wiley Online Library

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

Mechanistic investigation into phenol oxidation by IBX elucidated by DFT  calculations - Organic & Biomolecular Chemistry (RSC Publishing)  DOI:10.1039/C9OB02650A
Mechanistic investigation into phenol oxidation by IBX elucidated by DFT calculations - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB02650A

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

Chemistry of polyvalent iodine. - Abstract - Europe PMC
Chemistry of polyvalent iodine. - Abstract - Europe PMC

Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III)  reagents: an opportunity for rational catalyst design? - ScienceDirect
Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III) reagents: an opportunity for rational catalyst design? - ScienceDirect

Proposed mechanism for the oxidation of ortho substituted phenols by... |  Download Scientific Diagram
Proposed mechanism for the oxidation of ortho substituted phenols by... | Download Scientific Diagram

Pioneering Metal‐Free Oxidative Coupling Strategy of Aromatic Compounds  Using Hypervalent Iodine Reagents - Kita - 2015 - The Chemical Record -  Wiley Online Library
Pioneering Metal‐Free Oxidative Coupling Strategy of Aromatic Compounds Using Hypervalent Iodine Reagents - Kita - 2015 - The Chemical Record - Wiley Online Library

Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III)  reagents: an opportunity for rational catalyst design? - ScienceDirect
Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III) reagents: an opportunity for rational catalyst design? - ScienceDirect

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

Dearomatization strategies in the synthesis of complex natural products. -  Abstract - Europe PMC
Dearomatization strategies in the synthesis of complex natural products. - Abstract - Europe PMC

Iodosobenzene Diacetate
Iodosobenzene Diacetate

DFT mechanistic investigation into phenol dearomatization mediated by an  iodine(iii) reagent - Organic & Biomolecular Chemistry (RSC Publishing)
DFT mechanistic investigation into phenol dearomatization mediated by an iodine(iii) reagent - Organic & Biomolecular Chemistry (RSC Publishing)

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

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

Mechanistic investigation into phenol oxidation by IBX elucidated by DFT  calculations - Organic & Biomolecular Chemistry (RSC Publishing)  DOI:10.1039/C9OB02650A
Mechanistic investigation into phenol oxidation by IBX elucidated by DFT calculations - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C9OB02650A

Iodane - Wikiwand
Iodane - Wikiwand

Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III)  reagents: an opportunity for rational catalyst design? - ScienceDirect
Asymmetric oxidative dearomatizations promoted by hypervalent iodine(III) reagents: an opportunity for rational catalyst design? - ScienceDirect

Thermodynamics of Electrochemically Synthesized C-Nucleophiles for Reactive  CO2 Capture
Thermodynamics of Electrochemically Synthesized C-Nucleophiles for Reactive CO2 Capture

Proposed mechanism for the oxidation of ortho substituted phenols by... |  Download Scientific Diagram
Proposed mechanism for the oxidation of ortho substituted phenols by... | Download Scientific Diagram

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

Intramolecular α-Oxygenation of Amines via N-Heterocyclic Carbene-Catalyzed  Domino Reaction of Aryl Aldehyde: Experiment and DFT Calculation | CCS Chem
Intramolecular α-Oxygenation of Amines via N-Heterocyclic Carbene-Catalyzed Domino Reaction of Aryl Aldehyde: Experiment and DFT Calculation | CCS Chem

Commonly proposed mechanisms for the iodine(III)-mediated oxidation of... |  Download Scientific Diagram
Commonly proposed mechanisms for the iodine(III)-mediated oxidation of... | Download Scientific Diagram

Frontiers | Hypervalent Iodine Reagents in Palladium-Catalyzed Oxidative  Cross-Coupling Reactions | Chemistry
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
Synthesis of α-sulfonyloxyketones via iodobenzene diacetate (PIDA)-mediated oxysulfonyloxylation of alkynes with sulfonic acids - RSC Advances (RSC Publishing) DOI:10.1039/C7RA11875A

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

Phenyliodine(III) Diacetate (PIDA) Mediated Synthesis of Aromatic Azo  Compounds through Oxidative Dehydrogenative Coupling of Anilines: Scope and  Mechanism - Monir - 2014 - European Journal of Organic Chemistry - Wiley  Online Library
Phenyliodine(III) Diacetate (PIDA) Mediated Synthesis of Aromatic Azo Compounds through Oxidative Dehydrogenative Coupling of Anilines: Scope and Mechanism - Monir - 2014 - European Journal of Organic Chemistry - Wiley Online Library