Search Results - "König, Burkhard"
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Photocatalysis in Organic Synthesis – Past, Present, and Future
Published in European journal of organic chemistry (18-04-2017)“…The use of visible light as a catalyst in organic reactions has developed greatly in the last decade as a result of the increasing urge to implement…”
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Chromoselective Photocatalysis: Controlled Bond Activation through Light-Color Regulation of Redox Potentials
Published in Angewandte Chemie International Edition (27-06-2016)“…Catalysts that can be regulated in terms of activity and selectivity by external stimuli may allow the efficient multistep synthesis of complex molecules and…”
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3
The Photocatalyzed Meerwein Arylation: Classic Reaction of Aryl Diazonium Salts in a New Light
Published in Angewandte Chemie International Edition (26-04-2013)“…The use of diazonium salts for aryl radical generation and CH arylation processes has been known since 1896 when Pschorr first used the reaction for…”
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4
Birch‐Type Photoreduction of Arenes and Heteroarenes by Sensitized Electron Transfer
Published in Angewandte Chemie International Edition (01-10-2019)“…The direct reduction of arenes and heteroarenes by visible‐light irradiation remains challenging, as the energy of a single photon is not sufficient for…”
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Synthetic applications of eosin Y in photoredox catalysis
Published in Chemical communications (Cambridge, England) (01-01-2014)“…Eosin Y, a long known dye molecule, has recently been widely applied as a photoredox catalyst in organic synthesis. Low cost and good availability make eosin Y…”
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Synthetic Photoelectrochemistry
Published in Angewandte Chemie International Edition (13-07-2020)“…Photoredox catalysis (PRC) and synthetic organic electrochemistry (SOE) are often considered competing technologies in organic synthesis. Their fusion has been…”
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7
Visible Light Mediated Photoredox Catalytic Arylation Reactions
Published in Accounts of chemical research (16-08-2016)“…Introducing aryl- and heteroaryl moieties into molecular scaffolds are often key steps in the syntheses of natural products, drugs, or functional materials. A…”
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Strategies for the Photocatalytic Generation of Carbanion Equivalents for Reductant-Free C–C Bond Formations
Published in Accounts of chemical research (05-01-2021)“…Conspectus The use of photocatalysis in organic chemistry has encountered a surge of novel transformations since the start of the 21st century. The majority of…”
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9
Eosin Y Catalyzed Visible Light Oxidative C–C and C–P bond Formation
Published in Organic letters (05-08-2011)“…Eosin Y catalyzes efficiently the visible light mediated coupling of sp3 C–H bonds adjacent to the nitrogen atom in tetrahydroisoquinoline derivatives in the…”
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10
Chemical Degradation in Organic Light-Emitting Devices: Mechanisms and Implications for the Design of New Materials
Published in Advanced materials (Weinheim) (18-04-2013)“…Degradation of the materials in organic light‐emitting devices (OLEDs) is the major impediment for the development of economically feasible, highly efficient…”
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11
Reduction of aryl halides by consecutive visible light-induced electron transfer processes
Published in Science (American Association for the Advancement of Science) (07-11-2014)“…Biological photosynthesis uses the energy of several visible light photons for the challenging oxidation of water, whereas chemical photocatalysis typically…”
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12
Light-Induced Single-Electron Transfer Processes involving Sulfur Anions as Catalysts
Published in Journal of the American Chemical Society (29-09-2021)“…Photoredox catalysis has evolved as an attractive approach to enable a wide variety of chemical reactions with high selectivity under mild conditions. The…”
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13
Organic semiconductor photocatalyst can bifunctionalize arenes and heteroarenes
Published in Science (American Association for the Advancement of Science) (26-07-2019)“…Photoexcited electron-hole pairs on a semiconductor surface can engage in redox reactions with two different substrates. Similar to conventional…”
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14
Catalytic Generation of Carbanions through Carbonyl Umpolung
Published in Angewandte Chemie International Edition (27-09-2021)“…Carbonyl Umpolung is a powerful strategy in organic chemistry to construct complex molecules. Over the last few years, versatile catalytic approaches for the…”
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15
Sensitization‐Initiated Electron Transfer for Photoredox Catalysis
Published in Angewandte Chemie International Edition (10-07-2017)“…Photosynthetic organisms exploit antenna chromophores to absorb light and transfer excitation energy to the reaction center where redox reactions occur. In…”
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16
Photoredox Catalytic Organic Transformations using Heterogeneous Carbon Nitrides
Published in Angewandte Chemie International Edition (03-12-2018)“…Photoredox catalysis comprising homogeneous transition‐metal‐based systems, organic dyes, and semiconductors, has become a universal tool to catalyze a wide…”
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17
Photocatalytic formation of carbon-sulfur bonds
Published in Beilstein journal of organic chemistry (05-01-2018)“…This review summarizes recent developments in photocatalyzed carbon-sulfur bond formation. General concepts, synthetic strategies and the substrate scope of…”
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The Photocatalyzed Aza-Henry Reaction of N‑Aryltetrahydroisoquinolines: Comprehensive Mechanism, H•- versus H+‑Abstraction, and Background Reactions
Published in Journal of the American Chemical Society (14-09-2016)“…The cross-dehydrogenative coupling (CDC) reaction of N-aryltetrahydroisoquinolines (THIQ) is one of the most exploited photocatalytic transformation and a test…”
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19
Selective Single C(sp3)–F Bond Cleavage in Trifluoromethylarenes: Merging Visible-Light Catalysis with Lewis Acid Activation
Published in Journal of the American Chemical Society (27-12-2017)“…The conversion of easily available trifluoromethylarenes into aryldifluoromethyl compounds, which are valuable motifs in the pharmaceutical chemistry, is…”
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Excited State Anions in Organic Transformations
Published in Angewandte Chemie International Edition (15-03-2021)“…Utilizing light is a smart way to fuel chemical transformations as it allows the energy to be selectively focused on certain molecules. Many reactions…”
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