about
Photoredox Catalysis in Organic ChemistryDirect 1O2 optical excitation: A tool for redox biology.Lewis Acid Induced Toggle from Ir(II) to Ir(IV) Pathways in Photocatalytic Reactions: Synthesis of Thiomorpholines and Thiazepanes from Aldehydes and SLAP Reagents.The photophysics of photoredox catalysis: a roadmap for catalyst design.Functionalization of C-H Bonds by Photoredox Catalysis.Organocatalyzed Atom Transfer Radical Polymerization: Perspectives on Catalyst Design and Performance.Annulative π-Extension (APEX): Rapid Access to Fused Arenes, Heteroarenes, and Nanographenes.Photoredox-Mediated Routes to Radicals: The Value of Catalytic Radical Generation in Synthetic Methods Development.Cooperative Light-Activated Iodine and Photoredox Catalysis for the Amination of Csp3 -H Bonds.A General Small-Scale Reactor To Enable Standardization and Acceleration of Photocatalytic Reactions.Organocatalyzed Atom Transfer Radical Polymerization Using N-Aryl Phenoxazines as Photoredox Catalysts.Continuous Photo-Oxidation in a Vortex Reactor: Efficient Operations Using Air Drawn from the Laboratory.Direct C-H Cyanation of Arenes via Organic Photoredox CatalysisA Conjugated Microporous Polymer for Palladium-Free, Visible Light-Promoted Photocatalytic Stille-Type Coupling Reactions.Redox-Neutral Dual Functionalization of Electron-Deficient Alkenes.Mild, visible light-mediated decarboxylation of aryl carboxylic acids to access aryl radicals.Metal-free di- and tri-fluoromethylation of alkenes realized by visible-light-induced perylene photoredox catalysisVisible-light-induced oxidant and metal-free dehydrogenative cascade trifluoromethylation and oxidation of 1,6-enynes with waterA mild catalytic system for radical conjugate addition of nitrogen heterocycles.Electrosynthesis: A New Frontier in Aerobic Oxidation?Metal-free direct alkylation of unfunctionalized allylic/benzylic sp3 C-H bonds via photoredox induced radical cation deprotonation.Alkene Photo-Isomerization Inspired by VisionPhotoredox ketone catalysis for the direct C-H imidation and acyloxylation of arenes.Ketones as directing groups in photocatalytic sp3 C-H fluorination.The photochemical alkylation and reduction of heteroarenes.Generating hydrated electrons for chemical syntheses with a green LED.Recent developments in transition-metal photoredox-catalysed reactions of carbonyl derivatives.Mechanistic Insight into the Photocontrolled Cationic Polymerization of Vinyl Ethers.Synthesis of Arylamines via Aminium Radicals.Circumventing Intrinsic Metal Reactivity: Radical Generation with Redox-Active Ligands.Carboxylation of Aromatic and Aliphatic Bromides and Triflates with CO2 by Dual Visible-Light-Nickel Catalysis.Oxidative [1,2]-Brook Rearrangements Exploiting Single-Electron Transfer: Photoredox-Catalyzed Alkylations and Arylations.Sensitization-Initiated Electron Transfer for Photoredox Catalysis.Photosensitizer-free visible light-mediated gold-catalysed cis-difunctionalization of silyl-substituted alkynes.A Lewis Base Catalysis Approach for the Photoredox Activation of Boronic Acids and Esters.Photoredox Imino Functionalizations of Olefins.DHPA-Containing Cobalt-Based Redox Metal-Organic Cyclohelicates as Enzymatic Molecular Flasks for Light-Driven H2 Production.Selective Photooxidation Reactions using Water-Soluble Anthraquinone Photocatalysts.Aggregation-induced visible light absorption makes reactant 1,2-diisocyanoarenes act as photosensitizers in double radical isocyanide insertions.Bifunctional organic sponge photocatalyst for efficient cross-dehydrogenative coupling of tertiary amines to ketones.
P2860
Q28829372-F5BB1AD8-715D-4D30-A4CD-88CBBF3B174FQ33746305-BAF4F655-23CD-4C53-B3A1-AF22848E331BQ37609386-E11F1C5B-7637-4392-930B-87B07E7ADF1BQ38973647-2A018DC6-EB28-4453-A9DE-276211A2978FQ39079192-6111C2F5-FD26-4C83-8DEE-E55E57945E23Q39216091-C2811AF8-AE66-4088-8D28-79597A6E1AB4Q39216284-AA3F166B-48B2-499F-BEB3-73DB5611EC5CQ39245541-445E7DF3-F893-4F75-B7B3-28A4C8FC8DC9Q40951283-1477172F-ED20-499D-A40D-C05AE095D4E5Q40994194-1C2F2CB2-A2C6-4313-B76A-339480FB609DQ41036121-6314C951-4FE1-4851-8B0F-D11DDA61AE1BQ41121720-94E97972-0096-4941-AB48-F258B70DF198Q41230135-C5DB9EBC-A7FF-4FF3-B608-78F28800C902Q41483322-2230C403-EC2A-44D2-94C7-F003CCEC5C1CQ41541098-51CAEB77-6BF2-4714-83CC-942215C75A0BQ42098394-BCD3D246-82C8-44EB-82AB-E238BAE3EC77Q42278606-B43B73F4-A95A-4F76-A10A-75D83DDCB9B9Q42285443-DA409D9C-130B-4D57-9BD7-CB3E8D64C99AQ42289941-C8E2165A-14C3-41F9-8358-ACB9DABDAF58Q42338955-25B8808B-AD40-40DF-BAC5-44372BBD5334Q42365644-007225B7-0654-401B-850C-403824F9D896Q42367154-2DB35F6E-2AEA-4D46-BCCF-00445B3FF34AQ42367171-BA6D314E-424B-4B93-99E7-ED611DA891F5Q45929022-0AD8A2DA-A44F-4059-BE33-84D382A70086Q46230952-123881D9-F83F-4BEF-977E-91C4EDCF97B5Q46247882-5428349F-7C80-4018-82B6-64F449789FFCQ46264110-F9BC9EAC-E13B-4C13-8397-0E1BFD2AF916Q46292807-C691BAE1-BD9C-4CC7-94D0-5C4B8F8EB6CDQ46297455-4800AF3F-5344-4781-B346-B5EA4D2DAF92Q46311982-F889964A-1F27-4787-A1C2-112A1E67873FQ46317319-1BA5F0B5-8924-4583-86DA-EE7CAD456EEDQ46338286-A26F557F-529E-4B69-A0E9-F550EF31290CQ46360761-C222DC4E-7D55-415E-9849-84FA72698E5BQ46553062-F9D67585-F180-4A0A-AAAC-34DD6D0F868AQ47121098-D4FCA43B-47E0-4D5F-97AE-340C150D33A9Q47128255-56D16B81-6869-49AB-81FC-5EFAAEFE337EQ47137077-811C43EA-9BA2-4DE1-88A2-C3CFE34325A9Q47151123-EF5EE9BF-61EB-4581-8FEA-BC9E430CBD37Q47328790-1E457AE4-2A6D-415A-A42F-508499711B8DQ47375255-8018A072-0E92-47EC-B88A-44DEFE4BD469
P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Organic Photoredox Catalysis.
@en
type
label
Organic Photoredox Catalysis.
@en
prefLabel
Organic Photoredox Catalysis.
@en
P1433
P1476
Organic Photoredox Catalysis.
@en
P2093
David A Nicewicz
P304
10075-10166
P356
10.1021/ACS.CHEMREV.6B00057
P577
2016-06-10T00:00:00Z