0000000001301294

AUTHOR

Kazuhiro Chiba

showing 7 related works from this author

Innenrücktitelbild: Metall- und reagensfreie dehydrierende formale Benzyl-Aryl-Kreuzkupplung durch anodische Aktivierung in 1,1,1,3,3,3-Hexafluorprop…

2018

010405 organic chemistryChemistryGeneral Medicine010402 general chemistry01 natural sciences0104 chemical sciencesAngewandte Chemie
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Metal- and Reagent-Free Dehydrogenative Formal Benzyl-Aryl Cross-Coupling by Anodic Activation in 1,1,1,3,3,3-Hexafluoropropan-2-ol

2018

A selective dehydrogenative electrochemical functionalization of benzylic positions that employs 1,1,1,3,3,3-hexafluoropropan-2-ol (HFIP) has been developed. The electrogenerated products are versatile intermediates for subsequent functionalizations as they act as masked benzylic cations that can be easily activated. Herein, we report a sustainable, scalable, and reagent- and metal-free dehydrogenative formal benzyl-aryl cross-coupling. Liberation of the benzylic cation was accomplished through the use of acid. Valuable diarylmethanes are accessible in the presence of aromatic nucleophiles. The direct application of electricity enables a safe and environmentally benign chemical transformati…

Green chemistryChemical transformation010405 organic chemistryChemistryArylGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesMetalchemistry.chemical_compoundNucleophileReagentvisual_artvisual_art.visual_art_mediumSurface modificationAngewandte Chemie International Edition
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Metall- und reagensfreie dehydrierende formale Benzyl-Aryl-Kreuzkupplung durch anodische Aktivierung in 1,1,1,3,3,3-Hexafluorpropan-2-ol

2018

010405 organic chemistryChemistryGeneral Medicine010402 general chemistry01 natural sciences0104 chemical sciencesAngewandte Chemie
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Inside Back Cover: Metal- and Reagent-Free Dehydrogenative Formal Benzyl-Aryl Cross-Coupling by Anodic Activation in 1,1,1,3,3,3-Hexafluoropropan-2-o…

2018

Green chemistryChemistryArylGeneral ChemistryElectrochemistryMedicinal chemistryCatalysisAnodeCoupling (electronics)Metalchemistry.chemical_compoundvisual_artReagentvisual_art.visual_art_mediumAngewandte Chemie International Edition
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Dehydrogenative Anodic Cyanation Reaction of Phenols in Benzylic Positions

2019

Green chemistrychemistry.chemical_compoundChemistryElectrochemistryOrganic chemistryPhenolsCyanationElectrochemistryCatalysisAnodeChemElectroChem
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CCDC 1840041: Experimental Crystal Structure Determination

2018

Related Article: Yasushi Imada, Johannes L. Röckl, Anton Wiebe, Tile Gieshoff, Dieter Schollmeyer, Kazuhiro Chiba, Robert Franke, Siegfried R. Waldvogel|2018|Angew.Chem.,Int.Ed.|57|12136|doi:10.1002/anie.201804997

Space GroupCrystallography7-hydroxy-3-[(4-hydroxy-35-dimethylphenyl)methyl]-4-methyl-2H-1-benzopyran-2-oneCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1840040: Experimental Crystal Structure Determination

2018

Related Article: Yasushi Imada, Johannes L. Röckl, Anton Wiebe, Tile Gieshoff, Dieter Schollmeyer, Kazuhiro Chiba, Robert Franke, Siegfried R. Waldvogel|2018|Angew.Chem.,Int.Ed.|57|12136|doi:10.1002/anie.201804997

2-[(4-hydroxy-35-dimethylphenyl)methyl]-4-methoxy-7H-furo[32-g][1]benzopyran-7-oneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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