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Iodine-catalyzed transformation of molecules containing oxygen functional groups

Tetrahedron, 2011-02, Vol.67 (7), p.1355-1387

2011

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Reactivity of substrates with multiple competitive reactive sites toward NBS under neat reaction conditions promoted by visible light

Chemical papers, 2021-10, Vol.75 (10), p.5235-5248

2021

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NaSH-HCl mediated reduction of sulfoxides into sulfides under organic solvent-free reaction conditions

Green chemistry letters and reviews, 2020-10, Vol.13 (4), p.341-348

2020

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Highly atom-economic, catalyst- and solvent-free oxidation of sulfides into sulfones using 30% aqueous H2O2

Green chemistry : an international journal and green chemistry resource : GC, 2012, Vol.14 (11), p.3047-3052

JEREB, Marjan

2012

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Iodine-catalyzed Transformation of Aryl-substituted Alcohols Under Solvent-free and Highly Concentrated Reaction Conditions

Acta chimica Slovenica, 2017-12, Vol.64 (4), p.747-762

2017

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Oxidation of N -trifluoromethylthio sulfoximines using NaOCl·5H 2 O

Organic & biomolecular chemistry, 2024-03, Vol.22 (10), p.2012-2020

2024

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Oxidation of -trifluoromethylthio sulfoximines using NaOCl·5HO

Organic & biomolecular chemistry, 2024-03, Vol.22 (1), p.212-22

2024

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Oxidation of N-trifluoromethylthio sulfoximines using NaOCl·5H2O

Organic & biomolecular chemistry, 2024-03, Vol.22 (10), p.2012-2020

2024

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Effective and selective iodofunctionalisation of organic molecules in water using the iodine-hydrogen peroxide tandem

Chemical communications (Cambridge, England), 2004-11 (22), p.2614-2615

2004

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Conversion of thiols into sulfonyl halogenides under aerobic and metal-free conditions

Green chemistry : an international journal and green chemistry resource : GC, 2017, Vol.19 (9), p.2286-2295

2017

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Selective and Effective Fluorination of Organic Compounds in Water Using Selectfluor F-TEDA-BF4

Organic letters, 2004-12, Vol.6 (26), p.4973-4976

2004

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Dual behavior of alcohols in iodine-catalyzed esterification under solvent-free reaction conditions

Tetrahedron letters, 2009-05, Vol.50 (20), p.2347-2352

2009

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Sustainable and Selective Modern Methods of Noble Metal Recycling

Angewandte Chemie (International ed.), 2023-01, Vol.62 (5), p.e202214453-n/a

International ed. in English, 2023

Volltextzugriff (PDF)

Acid-promoted direct electrophilic trifluoromethylthiolation of phenols

Organic & biomolecular chemistry, 2015-03, Vol.13 (10), p.3103-3115

2015

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Electrophilic trifluoromethylthiolation of thiols with trifluoromethanesulfenamide

RSC advances, 2015-01, Vol.5 (72), p.58292-58306

2015

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Synthesis of trimethylsilyl carboxylates by HMDS under solvent-free conditions

Tetrahedron, 2016-09, Vol.72 (37), p.5713-5723

2016

Volltextzugriff (PDF)

Conversion of thiols into sulfonyl halogenides under aerobic and metal-free conditionsDedicated to Professor Emeritus Marko Zupan on the occasion of his 70th anniversary.Electronic supplementary information (ESI) available. See DOI: 10.1039/c7gc00556c

2017-05

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One-Pot Synthesis of N‑Iodo Sulfoximines from Sulfides

Journal of organic chemistry, 2021-04, Vol.86 (8), p.5991-6000

2021

Volltextzugriff (PDF)

Diversification of Trifluoromethylthiolation of Aromatic Molecules with Derivatives of Trifluoromethanesulfenamide

European journal of organic chemistry, 2018-08, Vol.2018 (27-28), p.3837-3843

2018

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Highly atom economical uncatalysed and I2-catalysed silylation of phenols, alcohols and carbohydrates, using HMDS under solvent-free reaction conditions (SFRC)

Tetrahedron, 2012-05, Vol.68 (20), p.3861-3867

Jereb, Marjan

2012

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TiIV-Catalyzed Asymmetric Sulfenylation of 1,3-Dicarbonyl Compounds

Chemistry : a European journal, 2007-11, Vol.13 (33), p.9384-9392

2007

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Acid-promoted direct electrophilic trifluoromethylthiolation of phenolsElectronic supplementary information (ESI) available: Copies of the 1H, 13C and 19F NMR spectra for all products. See DOI: 10.1039/c4ob02633k

2015-02

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Ti(IV)-catalyzed asymmetric sulfenylation of 1,3-dicarbonyl compounds

Chemistry : a European journal, 2007, Vol.13 (33), p.9384-9392

2007

Volltextzugriff (PDF)

Inside Cover: Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol (Angew. Chem. Int. Ed. 14/2022)

Angewandte Chemie International Edition, 2022-03, Vol.61 (14), p.n/a

2022

Volltextzugriff (PDF)

Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol

Angewandte Chemie (International ed.), 2022-03, Vol.61 (14), p.e202117587-n/a

International ed. in English, 2022

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Iodine-catalyzed transformation of molecules containing oxygen functional groups

Reactivity of substrates with multiple competitive reactive sites toward NBS under neat reaction conditions promoted by visible light

NaSH-HCl mediated reduction of sulfoxides into sulfides under organic solvent-free reaction conditions

Highly atom-economic, catalyst- and solvent-free oxidation of sulfides into sulfones using 30% aqueous H2O2

Iodine-catalyzed Transformation of Aryl-substituted Alcohols Under Solvent-free and Highly Concentrated Reaction Conditions

Oxidation of N -trifluoromethylthio sulfoximines using NaOCl·5H 2 O

Oxidation of -trifluoromethylthio sulfoximines using NaOCl·5HO

Oxidation of N-trifluoromethylthio sulfoximines using NaOCl·5H2O

Effective and selective iodofunctionalisation of organic molecules in water using the iodine-hydrogen peroxide tandem

Conversion of thiols into sulfonyl halogenides under aerobic and metal-free conditions

Selective and Effective Fluorination of Organic Compounds in Water Using Selectfluor F-TEDA-BF4

Dual behavior of alcohols in iodine-catalyzed esterification under solvent-free reaction conditions

Sustainable and Selective Modern Methods of Noble Metal Recycling

Acid-promoted direct electrophilic trifluoromethylthiolation of phenols

Electrophilic trifluoromethylthiolation of thiols with trifluoromethanesulfenamide

Synthesis of trimethylsilyl carboxylates by HMDS under solvent-free conditions

Conversion of thiols into sulfonyl halogenides under aerobic and metal-free conditionsDedicated to Professor Emeritus Marko Zupan on the occasion of his 70th anniversary.Electronic supplementary information (ESI) available. See DOI: 10.1039/c7gc00556c

One-Pot Synthesis of N‑Iodo Sulfoximines from Sulfides

Diversification of Trifluoromethylthiolation of Aromatic Molecules with Derivatives of Trifluoromethanesulfenamide

Highly atom economical uncatalysed and I2-catalysed silylation of phenols, alcohols and carbohydrates, using HMDS under solvent-free reaction conditions (SFRC)

TiIV-Catalyzed Asymmetric Sulfenylation of 1,3-Dicarbonyl Compounds

Acid-promoted direct electrophilic trifluoromethylthiolation of phenolsElectronic supplementary information (ESI) available: Copies of the 1H, 13C and 19F NMR spectra for all products. See DOI: 10.1039/c4ob02633k

Ti(IV)-catalyzed asymmetric sulfenylation of 1,3-dicarbonyl compounds

Inside Cover: Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol (Angew. Chem. Int. Ed. 14/2022)

Iodine‐Catalysed Dissolution of Elemental Gold in Ethanol

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