0000000000162249

AUTHOR

Stephan P. Blum

showing 12 related works from this author

Advances in photochemical and electrochemical incorporation of sulfur dioxide for the synthesis of value-added compounds.

2021

Organic photochemistry and electrochemistry currently receive tremendous attention in organic synthesis as both techniques enable the reagent-less activation of organic molecules without using expensive and hazardous redox reagents. The incorporation of SO2 into organic molecules is a relatively modern research topic, which likewise gains immense popularity since the discovery of the SO2 surrogate DABSO. Sulfur-containing organic molecules are omnipresent in pharmaceuticals and agrochemicals. This review covers the recent progress in electrochemical and photochemical methodologies for the incorporation and uses of SO2 in the synthesis of value-added compounds. Additionally, different work t…

010405 organic chemistryChemistryMechanistic organic photochemistryMetals and AlloysGeneral Chemistry010402 general chemistryPhotochemistryElectrochemistrycomplex mixtures01 natural sciencesRedoxCatalysisrespiratory tract diseases0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsOrganic moleculeschemistry.chemical_compoundMaterials ChemistryCeramics and CompositesOrganic synthesisSulfur dioxideChemical communications (Cambridge, England)
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Electrochemical nitration with nitrite

2021

Aromatic nitration has tremendous importance in organic chemistry as nitroaromatic compounds serve as versatile building blocks. This study represents the electrochemical aromatic nitration with NBu4 NO2 , which serves a dual role as supporting electrolyte and as a safe, readily available, and easy-to-handle nitro source. Stoichiometric amounts of 1,1,1-3,3,3-hexafluoroisopropan-2-ol (HFIP) in MeCN significantly increase the yield by solvent control. The reaction mechanism is based on electrochemical oxidation of nitrite to NO2 , which initiates the nitration reaction in a divided electrolysis cell with inexpensive graphite electrodes. Overall, the reaction is demonstrated for 20 examples w…

Green chemistryReaction mechanism540 Chemistry and allied sciencesSupporting electrolyteGeneral Chemical EngineeringElectrochemistryCombinatorial chemistrySolventchemistry.chemical_compoundGeneral EnergychemistryNitrationYield (chemistry)540 ChemieEnvironmental ChemistryGeneral Materials ScienceNitrite
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Metallfreie, elektrochemische Synthese von Sulfonamiden direkt aus (Hetero)arenen, SO 2 und Aminen

2021

ChemistryGeneral MedicineAngewandte Chemie
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Metal- and Reagent-Free Electrochemical Synthesis of Alkyl Arylsulfonates in a Multi-Component Reaction.

2020

Abstract This work presents the first electrochemical preparation of alkyl arylsulfonates by direct anodic oxidation of electron‐rich arenes. The reaction mechanism features a multi‐component reaction consisting of electron‐rich arenes, an alcohol of choice and excess SO2 in an acetonitrile‐HFIP reaction mixture. In‐situ formed monoalkyl sulfites are considered as key intermediates with bifunctional purpose. Firstly, this species functions as nucleophile and secondly, excellent conductivity is provided. Several primary and secondary alcohols and electron‐rich arenes are implemented in this reaction to form the alkyl arylsulfonates in yields up to 73 % with exquisite selectivity. Boron‐doped…

Reaction mechanismoxidationAlcohol010402 general chemistry01 natural sciencesCatalysisC−H activationchemistry.chemical_compoundradical ionsNucleophileMulti-component reactionElectrochemistryBifunctionalAlkylchemistry.chemical_classification010405 organic chemistrygreen chemistryCommunicationOrganic ChemistryGeneral ChemistryCombinatorial chemistryCommunications0104 chemical scienceschemistryReagentSelectivityChemistry (Weinheim an der Bergstrasse, Germany)
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Frontispiece: Metal‐Free Electrochemical Synthesis of Sulfonamides Directly from (Hetero)arenes, SO 2 , and Amines

2021

Green chemistryMetal freeChemistryGeneral ChemistryElectrochemistryCombinatorial chemistryCatalysisAngewandte Chemie International Edition
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Cover Feature: Metal‐ and Reagent‐Free Electrochemical Synthesis of Alkyl Arylsulfonates in a Multi‐Component Reaction (Chem. Eur. J. 38/2020)

2020

chemistry.chemical_classificationGreen chemistryChemistryOrganic ChemistryGeneral ChemistryElectrochemistryCombinatorial chemistryCatalysisArylsulfonatesMetalReagentvisual_artMulti-component reactionvisual_art.visual_art_mediumCover (algebra)AlkylChemistry – A European Journal
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Metal‐Free Electrochemical Synthesis of Sulfonamides Directly from (Hetero)arenes, SO2, and Amines

2021

Abstract Sulfonamides are among the most important chemical motifs in pharmaceuticals and agrochemicals. However, there is no methodology to directly introduce the sulfonamide group to a non‐prefunctionalized aromatic compound. Herein, we present the first dehydrogenative electrochemical sulfonamide synthesis protocol by exploiting the inherent reactivity of (hetero)arenes in a highly convergent reaction with SO2 and amines via amidosulfinate intermediate. The amidosulfinate serves a dual role as reactant and supporting electrolyte. Direct anodic oxidation of the aromatic compound triggers the reaction, followed by nucleophilic attack of the amidosulfinate. Boron‐doped diamond (BDD) electro…

chemistry.chemical_classificationGreen chemistryradical reactions010405 organic chemistrySupporting electrolytegreen chemistryoxidationCommunicationGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysisCommunications0104 chemical sciencesSulfonamideSolventchemistryNucleophileElectrochemistry | Hot PaperelectrochemistrysulfonamidesElectrodeReactivity (chemistry)Angewandte Chemie (International Ed. in English)
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Electrochemical synthesis of sulfamides.

2021

Herein we demonstrate the first electrochemical synthesis protocol of symmetrical sulfamides directly from anilines and SO2 mediated by iodide. Sulfamides are an emerging functional group in drug design. Highlights are the direct use of SO2 from a stock solution and no necessity of any supporting electrolyte. Overall, the reaction has been demonstrated for 15 examples with yields up to 93%.

chemistry.chemical_classificationChemistrySupporting electrolyteIodideMetals and AlloysGeneral ChemistryElectrochemistrycomplex mixturesCombinatorial chemistryCatalysisrespiratory tract diseasesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundFunctional groupMaterials ChemistryCeramics and CompositesStock solutionChemical communications (Cambridge, England)
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Frontispiz: Metallfreie, elektrochemische Synthese von Sulfonamiden direkt aus (Hetero)arenen, SO 2 und Aminen

2021

General MedicineAngewandte Chemie
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CCDC 2070594: Experimental Crystal Structure Determination

2021

Related Article: Stephan P. Blum, Lukas Schäffer, Dieter Schollmeyer, Siegfried R. Waldvogel|2021|Chem.Commun.|57|4775|doi:10.1039/D1CC01428E

NN'-bis(4-(22-dimethylethyl)phenyl)sulfamideSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2032478: Experimental Crystal Structure Determination

2021

Related Article: Stephan P. Blum, Tarik Karakaya, Dieter Schollmeyer, Artis Klapars, Siegfried R. Waldvogel|2021|Angew.Chem.,Int.Ed.|60|5056|doi:10.1002/anie.202016164

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters4-(345-trimethoxybenzene-1-sulfonyl)morpholineExperimental 3D Coordinates
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CCDC 1988057: Experimental Crystal Structure Determination

2020

Related Article: Stephan P. Blum, Dieter Schollmeyer, Maris Turks, Siegfried R. Waldvogel|2020|Chem.-Eur.J.|26|8358|doi:10.1002/chem.202001180

Space GroupCrystallography22-dimethylpropyl 345-trimethoxybenzene-1-sulfonateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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