Generation of electrophilic iodine from iodine monochloride in neutral media. Iodination and protodeiodination of carbazone; Russian Journal of Organic Chemistry; Vol. 39, № 6

Generation of electrophilic iodine from iodine monochloride in neutral media. Iodination and protodeiodination of carbazone; Russian Journal of Organic Chemistry; Vol. 39, № 6

Bibliographische Detailangaben
Parent link:	Russian Journal of Organic Chemistry.— , 1956- Vol. 39, № 6.— 2003.— P. 875-880
1. Verfasser:	Filimonov V. D. Viktor Dmitrievich
Weitere Verfasser:	Krasnokutskaya E. A., Lesina Yu. A.
Zusammenfassung:	In reaction of iodine monochloride with CF3COOAg, CH 3COONa or (CH3COO)2Pb in acetonitrile and acetic acid the chloride is bonded by metal cations, and electrophilic iodine is generated able to easily iodinate anthracene and carbazole. However at the iodination of anthracene in the presence of oxygen the prevailing process is anthracene oxidation to anthraquinone. In the presence of sulfuric acid protodeiodination of 3-iodocarbazole was found to occur resulting in rearranged products. В фонде НТБ ТПУ отсутствует
Sprache:	Englisch
Veröffentlicht:	2003
Schlagworte:	труды учёных ТПУ
Format:	Buchkapitel
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=596555

Ähnliche Einträge

Iodination of aromatic compounds with iodine monochloride in aqueous sulfuric acid; Russian Journal of Organic Chemistry; Vol. 36, № 5
Veröffentlicht: (2000)

New methods of generation of electrophilic iodine in neutral and weakly acidic media; Korus 2002; Vol. 1
Veröffentlicht: (2002)

Iodination and chlorination of aromatic polycyclic hydrocarbons with iodine monochloride in aqueous sulfuric acid; Russian Journal of Organic Chemistry; Vol. 37, iss. 8
von: Chaikovskii V. K. Vitold Kazimirovich
Veröffentlicht: (2001)

Iodination of Deactivated Aromatic Compounds with Iodine Chloride; Russian Journal of Organic Chemistry; Vol. 34, № 7
Veröffentlicht: (1998)

Iodination of nitroarenes by a superactive reagent based on iodine chloride; Russian Chemical Bulletin; Vol. 48, № 7
von: Chaikovskii V. K. Vitold Kazimirovich
Veröffentlicht: (1999)

Benziodoxole-Derived Organosulfonates: The Strongest Hypervalent Iodine Electrophiles and Oxidants; Synlett; Vol. 31, № 4
Veröffentlicht: (2020)

Superactive iodination reagent on a base of iodine chloride and silver sulfate; Synthesis; № 5
Veröffentlicht: (1999)

Solid-phase iodination of arenes with the system iodine-diacetoxy(phenyl)- λ3-iodane; Russian Journal of Organic Chemistry; Vol. 41, iss. 12
von: Krasnokutskaya E. A . Elena Aleksandrovna
Veröffentlicht: (2005)

The high-power Iodine laser
von: Brederlow G.
Veröffentlicht: (Berlin, Springer-Verlag, 1983)

Facile iodination of aromatic compounds having electron-withdrawing substituents. Generation of triiodine cation in the system tetra-N- iodoglycoluril-iodine-sulfuric acid; Russian Journal of Organic Chemistry; Vol. 44, iss. 6
Veröffentlicht: (2008)

Theoretical analysis of reactions of electrophilic iodination and chlorination of benzene and polycyclic arenes in density functional theory approximation; Russian Journal of Organic Chemistry; Vol. 44, iss. 5
Veröffentlicht: (2008)

DFT investigation of the thermodynamics and mechanism of electrophilic chlorination and iodination of arenes; Journal of Molecular Modeling; Vol. 17, iss. 11
Veröffentlicht: (2011)

Evaluation of the reactivity and regioselectivity of superelectrophilic iodinating systems; Russian Journal of Organic Chemistry; Vol. 45, iss. 9
von: Chaikovskii V. K. Vitold Kazimirovich
Veröffentlicht: (2009)

A Novel Iodination of Aromatic Rings Using Iodine/Metallic Nitrate; Bulletin of the Korean Chemical Society; Vol. 19, iss. 4
Veröffentlicht: (1998)

Synthetic applications of pseudocyclic hypervalent iodine compounds; Organic and Biomolecular Chemistry; Vol. 14
von: Yoshimura A. Akira
Veröffentlicht: (2016)

Hypervalent Iodine Reagents for Green Synthesis; Dombay Organic Conference Cluster, DOCC-2016
Veröffentlicht: (2016)

m-Iodosylbenzoic acid as a convenient recyclable hypervalent iodine oxidant for the synthesis of α-iodo ketones by oxidative iodination of ketones; Synthesis; № 21
Veröffentlicht: (2010)

Cyclotron Production of Iodine-124; Russian Physics Journal; Vol. 62, iss. 12
von: Salodkin S. S. Stepan Sergeevich
Veröffentlicht: (2020)

Iodination and iodonitration of phenylacetylene under solvent-free conditions; Russian Journal of Organic Chemistry; Vol. 43, iss. 1
Veröffentlicht: (2007)

Synthesis of hypervalent iodine salts for the functionalization of carbohydrates; СХС-2025
von: Amhanokhai E. A.
Veröffentlicht: (2025)

Superactive and economical reagent for iodination of arens; Korus`98. Abstracts
von: Chaikovski V. K.
Veröffentlicht: (1998)

Comparative study of the reactivity of iodinating agents in solution and solid phase; Russian Journal of Organic Chemistry; Vol. 41, iss. 6
Veröffentlicht: (2005)

Preparation, Structure, and Reactivity of Pseudocyclic Benziodoxole Tosylates: New Hypervalent Iodine Oxidants and Electrophiles; Chemistry - A European Journal; Vol. 23, iss. 3
Veröffentlicht: (2017)

Structure and reactivity of powerful water-soluble oxidizing hypervalent iodine reagents; Markovnikov Congress on Organic Chemistry
Veröffentlicht: (2019)

Hypervalent Iodine-Mediated Azidation Reactions; European Journal of Organic Chemistry; Vol. 2022, iss. 34
Veröffentlicht: (2022)

Voltammetry behavior of iodine and selenium on new organo-modified electrodes: Development of a procedure for the determination of iodine and selenium; Journal of Analytical Chemistry; Vol. 68, iss. 10
Veröffentlicht: (2013)

Hypervalent Iodine(III) Reagent Mediated Regioselective Cycloaddition of Aldoximes with Enaminones; European Journal of Organic Chemistry; Vol. 2019, iss. 39
Veröffentlicht: (2019)

Oligomeric iodosylbenzene sulfate: a convenient hypervalent iodine reagent for oxidation of organic sulfides and alkenes; Synthesis; № 15
Veröffentlicht: (2009)

Comparative analysis of a full-electron basis set and pseudopotential for the iodine atom in DFT quantum-chemical calculations of iodine-containing compounds; Journal of Structural Chemistry; Vol. 49, № 3
von: Yurieva A. G.
Veröffentlicht: (2008)

Design of new hypervalent iodine azidating reagents: synthesis and properties; Mendeleev 2021
Veröffentlicht: (2021)

Synthesys of Magnetically-controlled Reusable Catalyst of Alcohol's Oxidation Process Based on Polyvalent Iodine; Current topics in Organic Chemistry
von: Gromov M. V. Maksim Valerievich
Veröffentlicht: (2015)

Access to Carbonyl Azides via Iodine(III)-Mediated Cross-Coupling; Organic Letters; Vol. 26, iss. 43
Veröffentlicht: (2024)

1,3-Diiodo-5,5-dimethylhydantoin-An efficient reagent for iodination of aromatic compounds; Russian Journal of Organic Chemistry; Vol. 43, iss. 9
Veröffentlicht: (2007)

Iodine Monoacetate for Efficient Oxyiodinations of Alkenes and Alkynes; Synlett; Vol. 29, iss. 4
Veröffentlicht: (2018)

Cathodoluminescence of iodine dimers in KCl:I crystals; Optics and Spectroscopy; Vol. 98, № 3
Veröffentlicht: (2005)

Application of hypervalent iodine compounds in advanced green technologies; Resource-Efficient Technologies; No 1
von: Zhdankin V. V.
Veröffentlicht: (2021)

Hypervalent iodine compounds: synthesis, structure and its applications in aqueous media; Химия и химическая технология в XXI веке
Veröffentlicht: (2020)

Preparation, structure, and reactivity of bicyclic benziodazole: a new hypervalent iodine heterocycle; Beilstein Journal of Organic Chemistry; Vol. 14
Veröffentlicht: (2018)

Supramolecular Organization of Diaryliodonium Dicyanoargentates(I) Provided by Iodine(III)–Cyanide Halogen Bonding; Inorganics; Vol. 13, iss. 5
Veröffentlicht: (2025)

Oxidative cycloaddition of hydroxamic acids with dienes or guaiacols mediated by iodine(III) reagents; Beilstein Journal of Organic Chemistry; Vol. 14
Veröffentlicht: (2018)