Enantioselective C-H functionalization using high-valent group 9 metal catalysts
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- 資料種別
- 記事
- 著者・編者
- Tatsuhiko Yoshino
- 出版年月日等
- 2022-07-08
- 出版年（W3CDTF）
- 2022-07-08
- タイトル（掲載誌）
- Bulletin of the Chemical Society of Japan
- 巻号年月日等（掲載誌）
- 95(8)
- 掲載巻
- 95(8)
- ISSN（掲載誌）
- 1348-0634
- ISSN-L（掲載誌）
- 0009-2673
- 本文の言語コード
- eng
- DOI
- 10.1246/bcsj.20220168
- 国立国会図書館永続的識別子
- info:ndljp/pid/12686449
- コレクション（共通）
- コレクション（障害者向け資料：レベル1）
- コレクション（個別）
- 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
- 収集根拠
- オンライン資料収集制度
- 受理日（W3CDTF）
- 2023-03-07T17:43:09+09:00
- 保存日（W3CDTF）
- 2023-01-20
- 記録形式（IMT）
- application/pdf
- オンライン閲覧公開範囲
- 国立国会図書館内限定公開
- デジタル化資料送信
- 図書館・個人送信対象外
- 遠隔複写可否（NDL）
- 可
- 掲載誌（国立国会図書館永続的識別子）
- info:ndljp/pid/12686446
- 連携機関・データベース
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- 要約等
- コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
- DOI
- 10.1246/bcsj.20220168
- 関連情報（URI）
- 参照
- Enantioselective C-H amidation of sulfondiimines for the synthesis of 1,2,4-benzothiadiazine-1-imines under cobalt catalysisEnantioselective Synthesis of 1,2‐Benzothiazine 1‐Imines via Ru<sup>II</sup>/Chiral Carboxylic Acid‐Catalyzed C−H Alkylation/Cyclization
- 参照
- Cp*Co<sup>III</sup>-catalyzed directed C–H trifluoromethylthiolation of 2-phenylpyridines and 6-arylpurinesCp*M-Catalyzed Direct Annulation with Terminal Alkynes and Their Surrogates for the Construction of Multi-Ring SystemsCp*Rh<sup>III</sup>/Chiral Disulfonate/CuOAc Catalyst System for the Enantioselective Intramolecular Oxyamination of AlkenesCp*Co (III) -Catalyzed C-H Functionalization and Asymmetric Reactions Using External Chiral SourcesChiral Carboxylic Acid Enabled Achiral Rhodium(III)‐Catalyzed Enantioselective C−H FunctionalizationSynthesis of 1,1′‐Spirobiindane‐7,7′‐Disulfonic Acid and Disulfonimide: Application for Catalytic Asymmetric AminalizationChemInform Abstract: Oxidative Coupling of Aromatic Substrates with Alkynes and Alkenes under Rhodium CatalysisRuthenium(II)/Chiral Carboxylic Acid Catalyzed Enantioselective C-H Functionalization of SulfoximinesCp*Co<sup>III</sup>/Chiral Carboxylic Acid‐Catalyzed Enantioselective 1,4‐Addition Reactions of Indoles to MaleimidesChiral 2-Aryl Ferrocene Carboxylic Acids for the Catalytic Asymmetric C(sp<sup>3</sup>)–H Activation of ThioamidesCatalytic Enantioselective Methylene C(sp<sup>3</sup>)−H Amidation of 8‐Alkylquinolines Using a Cp*Rh<sup>III</sup>/Chiral Carboxylic Acid SystemPentamethylcyclopentadienyl rhodium(III)-chiral disulfonate hybrid catalysis for enantioselective C-H bond functionalizationChemInform Abstract: Cp*Co<sup>III</sup> Catalyzed Site‐Selective C—H Activation of Unsymmetrical O‐Acyl Oximes: Synthesis of Multisubstituted Isoquinolines from Terminal and Internal Alkynes.(Pentamethylcyclopentadienyl)cobalt(III)‐Catalyzed C–H Bond Functionalization: From Discovery to Unique Reactivity and SelectivityA Cationic High‐Valent Cp*Co<sup>III</sup> Complex for the Catalytic Generation of Nucleophilic Organometallic Species: Directed CH Bond ActivationPyrroloindolone Synthesis via a Cp*Co<sup>III</sup>-Catalyzed Redox-Neutral Directed C–H Alkenylation/Annulation SequenceStereoselective Synthesis of Tetrasubstituted Alkenes via a Cp*Co<sup>III</sup>‐Catalyzed C−H Alkenylation/Directing Group Migration SequenceAsymmetric Net Cycloaddition for Access to Diverse Substituted 1,5-BenzothiazepinesRhodium(III)/Chiral Carboxylic Acid Catalyzed Enantioselective C(sp<sup>3</sup>)–H Alkylation of 8-Ethylquinolines with α,β-Unsaturated Carbonyl CompoundsMild metal-catalyzed C–H activation: examples and conceptsChiral Cyclopentadienyls: Enabling Ligands for Asymmetric Rh(III)-Catalyzed C–H FunctionalizationsChiral Cyclopentadienyl Ligands as Stereocontrolling Element in Asymmetric C–H FunctionalizationEnantioselective Formal C(sp<sup>3</sup>)−H Bond Activation in the Synthesis of Bioactive Spiropyrazolone DerivativesRuthenium(II)‐Catalyzed Asymmetric Inert C−H Bond Activation Assisted by a Chiral Transient Directing GroupComputational Studies of Carboxylate-Assisted C–H Activation and Functionalization at Group 8–10 Transition Metal CentersAchiral Cp*Rh(III)/Chiral Lewis Base Cooperative Catalysis for Enantioselective Cyclization via C–H ActivationCobalt(III)‐Catalyzed Enantioselective Intermolecular Carboamination by C−H FunctionalizationSynthesis and blood pressure lowering activity of 3-(substituted-amino)-1,2,4-benzothiadiazine 1-oxide derivativesPalladium-Catalyzed Enantioselective β-C(sp<sup>3</sup>)–H Activation Reactions of Aliphatic Acids: A Retrosynthetic Surrogate for Enolate Alkylation and Conjugate AdditionCobalt(III)/Chiral Carboxylic Acid‐Catalyzed Enantioselective Synthesis of Benzothiadiazine‐1‐oxides via C−H ActivationAir‐Stable Carbonyl(pentamethylcyclopentadienyl)cobalt Diiodide Complex as a Precursor for Cationic (Pentamethylcyclopentadienyl)cobalt(III) Catalysis: Application for Directed C‐2 Selective CH Amidation of IndolesCp*Co<sup>III</sup>-Catalyzed Dehydrative C–H Allylation of 6-Arylpurines and Aromatic Amides Using Allyl Alcohols in Fluorinated AlcoholsOverview of the Mechanistic Work on the Concerted Metallation–Deprotonation PathwayDiverse Approaches for Enantioselective C−H Functionalization Reactions Using Group 9 Cp<sup>x</sup>M<sup>III</sup> CatalystsPalladium-Catalyzed Transformations of Alkyl C–H BondsCp*Co(III)/MPAA-Catalyzed Enantioselective Amidation of Ferrocenes Directed by Thioamides under Mild ConditionsPalladium-Catalyzed Asymmetric Arylation of C(sp<sup>3</sup>)–H Bonds of Aliphatic Amides: Controlling Enantioselectivity Using Chiral Phosphoric Amides/AcidsAsymmetric Counteranion‐Directed CatalysisEnantioselective Ruthenium-Catalyzed C–H Alkylations by a Chiral Carboxylic Acid with Attractive Dispersive InteractionsCp*Co(III)-Catalyzed Enantioselective Hydroarylation of Unactivated Terminal Alkenes via C–H ActivationPyridinium 1,1′-Binaphthyl-2,2′-disulfonates as Highly Effective Chiral Brønsted Acid−Base Combined Salt Catalysts for Enantioselective Mannich-Type ReactionCobalt-catalyzed Synthesis of Homoallylic Amines from Imines and Terminal AlkenesWeinreb Amide Directed Versatile C−H Bond Functionalization under (η<sup>5</sup>‐Pentamethylcyclopentadienyl)cobalt(III) CatalysisSite- and Regioselective Monoalkenylation of Pyrroles with Alkynes via Cp*Co<sup>III</sup> CatalysisOne-Step Synthesis of 4H-3,1-Benzoxazin-4-ones from Weinreb Amides and 1,4,2-Dioxazol-5-ones via Cobalt-Catalyzed C–H Bond ActivationDevelopment of Pseudo-<i>C</i><sub>2</sub>-symmetric Chiral Binaphthyl Monocarboxylic Acids for Enantioselective C(sp<sup>3</sup>)–H Functionalization Reactions under Rh(III) CatalysisRhodium- and Iridium-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes via Regioselective C−H Bond CleavageManipulating the Diastereoselectivity of Ortholithiation in Planar Chiral FerrocenesRuthenium Complex-Catalyzed Direct Ortho Arylation and Alkenylation of 2-Arylpyridines with Organic HalidesSynthesis of amino acids and peptides with bulky side chains <i>via</i> ligand-enabled carboxylate-directed γ-C(sp<sup>3</sup>)–H arylationElectronic and Steric Tuning of a Prototypical Piano Stool Complex: Rh(III) Catalysis for C–H FunctionalizationEnantioselective Cobalt(III)‐Catalyzed C−H Activation Enabled by Chiral Carboxylic Acid CooperationA Powerful Chiral Counterion Strategy for Asymmetric Transition Metal CatalysisDual-Ligand-Enabled Ir(III)-Catalyzed Enantioselective C–H Amidation for the Synthesis of Chiral SulfoxidesTransition‐Metal‐Catalyzed Selective Functionalization of C(sp<sup>3</sup>)−H Bonds in Natural ProductsChiral Carboxylic Acid Assisted Enantioselective C–H Activation with Achiral Cp<sup>x</sup>M<sup>III</sup> (M = Co, Rh, Ir) CatalystsEfficient Synthesis of Sulfur-Stereogenic Sulfoximines via Ru(II)-Catalyzed Enantioselective C–H Functionalization Enabled by Chiral Carboxylic Acidα,β-Unsaturated acyl ammonium species as reactive intermediates in organocatalysis: an updateForging C−heteroatom bonds by transition-metal-catalyzed enantioselective C–H functionalizationChiral Arene Ligand as Stereocontroller for Asymmetric C−H Activation**Dehydrative Direct CH Allylation with Allylic Alcohols under [Cp*Co<sup>III</sup>] CatalysisEnantioselective C(sp<sup>3</sup>)–H Amidation of Thioamides Catalyzed by a Cobalt<sup>III</sup>/Chiral Carboxylic Acid Hybrid SystemFacile Net Cycloaddition Approach to Optically Active 1,5-BenzothiazepinesStrategic evolution in transition metal-catalyzed directed C–H bond activation and future directionsEnantioselective amine α-functionalization via palladium-catalysed C–H arylation of thioamidesAsymmetric Organocatalysis: The Emerging Utility of α,β‐Unsaturated Acylammonium SaltsPalladium-Catalyzed Enantioselective C–H Activation of Aliphatic Amines Using Chiral Anionic BINOL-Phosphoric Acid LigandsThe Importance of 1,5‐Oxygen⋅⋅⋅Chalcogen Interactions in Enantioselective Isochalcogenourea CatalysisEnantioselective C(sp <sup>3</sup> )‒H bond activation by chiral transition metal catalystsRh-Catalyzed Intermolecular Carbenoid Functionalization of Aromatic C–H Bonds by α-DiazomalonatesCp<sup><i>x</i></sup>M(<scp>iii</scp>)-catalyzed enantioselective C–H functionalization through migratory insertion of metal–carbenes/nitrenesStereoselective pharmacological effects and benzodiazepine receptor affinity of the enantiomers of Gö 4962Cobalt(III)-Catalyzed Diastereo- and Enantioselective Three-Component C–H FunctionalizationC–H activationAsymmetric C–H Activation for the Synthesis of P- and Axially Chiral Biaryl Phosphine Oxides by an Achiral Cp*Ir Catalyst with Chiral Carboxylic AmideEnantioselective C−H Activation with Earth‐Abundant 3d Transition MetalsLigand effects on the stereochemistry of the metalation of chiral ferrocenyloxazolinesChiral Cyclopentadienyl Cobalt(III) Complexes Enable Highly Enantioselective 3d-Metal-Catalyzed C–H FunctionalizationsAn Enantioselective Bidentate Auxiliary Directed Palladium‐Catalyzed Benzylic C−H Arylation of Amines Using a BINOL Phosphate LigandRuthenium(II)-Catalyzed C–H Bond Activation and FunctionalizationThe role of non-nucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection1Presented at the Eleventh International Conference on Antiviral Research, San Diego, CA, 5–10 April 1998.1Substrate Activation Strategies in Rhodium(III)-Catalyzed Selective Functionalization of ArenesThioamide‐Directed Cobalt(III)‐Catalyzed Selective Amidation of C(sp<sup>3</sup>)−H BondsPalladium(II)‐Catalyzed Enantioselective Arylation of Unbiased Methylene C(sp<sup>3</sup>)−H Bonds Enabled by a 2‐Pyridinylisopropyl Auxiliary and Chiral Phosphoric AcidsCarboxylate-Assisted Ruthenium-Catalyzed Alkyne Annulations by C–H/Het–H Bond FunctionalizationsWeakly Coordinating Directing Groups for Ruthenium(II)‐ Catalyzed CH ActivationImidate as the Intact Directing Group for the Cobalt-Catalyzed C–H AllylationIntroducing the Chiral Transient Directing Group Strategy to Rhodium(III)‐Catalyzed Asymmetric C−H ActivationMechanistic view of Ru-catalyzed C–H bond activation and functionalization: computational advancesApplications of Chiral Cyclopentadienyl (Cp<sup>x</sup>) Metal Complexes in Asymmetric CatalysisRuthenium-catalysed σ-activation for remote <i>meta</i>-selective C–H functionalisationPalladium(0)-catalyzed asymmetric C(sp<sup>3</sup>)–H arylation using a chiral binol-derived phosphate and an achiral ligandChiral Transient Directing Groups in Transition-Metal-Catalyzed Enantioselective C–H Bond FunctionalizationChiral Counteranions in Asymmetric Transition-Metal Catalysis: Highly Enantioselective Pd/Brønsted Acid-Catalyzed Direct α-Allylation of AldehydesCarboxylate-Assisted Transition-Metal-Catalyzed C−H Bond Functionalizations: Mechanism and Scope<i>ortho</i>‐C−H Arylation of Benzoic Acids with Aryl Bromides and Chlorides Catalyzed by RutheniumRecent Development on Cp*Ir(III)‐Catalyzed C−H Bond FunctionalizationRuthenium-Catalyzed Enantioselective C–H Functionalization: A Practical Access to Optically Active Indoline DerivativesAchiral Cp<sup>x</sup>Ir(III)/Chiral Carboxylic Acid Catalyzed Enantioselective C–H Amidation of Ferrocenes under Mild ConditionsAsymmetric Counteranion‐Directed Catalysis: Concept, Definition, and ApplicationsEnantioselective Synthesis of Chiral‐at‐Sulfur 1,2‐Benzothiazines by Cp<sup>x</sup>Rh<sup>III</sup>‐Catalyzed C−H Functionalization of SulfoximinesFrom Pd(OAc)<sub>2</sub> to Chiral Catalysts: The Discovery and Development of Bifunctional Mono-N-Protected Amino Acid Ligands for Diverse C–H Functionalization ReactionsRhodium(III)‐Catalyzed Activation of CH Bonds and Subsequent Intermolecular Amidation at Room TemperatureBiotinylated Rh(III) Complexes in Engineered Streptavidin for Accelerated Asymmetric C–H ActivationAn Efficient Waste-Free Oxidative Coupling via Regioselective C−H Bond Cleavage: Rh/Cu-Catalyzed Reaction of Benzoic Acids with Alkynes and Acrylates under AirCooperative Effects between Chiral Cp<sup>x</sup>–Iridium(III) Catalysts and Chiral Carboxylic Acids in Enantioselective C−H Amidations of Phosphine OxidesMicrowave-Assisted Cp*Co<sup>III</sup>-Catalyzed C–H Activation/Double C–N Bond Formation Reactions to Thiadiazine 1-OxidesRhodium‐Catalyzed Enantioselective Synthesis of β‐Amino Alcohols via Desymmetrization of <i>gem</i>‐Dimethyl GroupsCobalt-Catalyzed C–H ActivationThe Catalytic Acylcyanation of IminesFormal S<sub>N</sub>‐Type Reactions in Rhodium(III)‐Catalyzed CH Bond ActivationMechanistic Studies on the Rh(III)-Mediated Amido Transfer Process Leading to Robust C–H Amination with a New Type of Amidating ReagentDual role of carboxylic acid additive: mechanistic studies and implication for the asymmetric C–H amidationDioxazolones: Stable Substrates for the Catalytic Transfer of Acyl NitrenesBiological and biochemical anti-HIV activity of the benzothiadiazine class of nonnucleoside reverse transcriptase inhibitorsA Tunable Class of Chiral Cp Ligands for Enantioselective Rhodium(III)-Catalyzed C–H Allylations of BenzamidesComparison of the Reactivities and Selectivities of Group 9 [Cp*M<sup>III</sup>] Catalysts in C−H Functionalization ReactionsPd<sup>II</sup>‐Catalyzed Enantioselective Activation of C(sp<sup>2</sup>)H and C(sp<sup>3</sup>)H Bonds Using Monoprotected Amino Acids as Chiral LigandsTransition-Metal-Catalyzed C–H Bond Addition to Carbonyls, Imines, and Related Polarized π BondsThe Importance of Kinetic and Thermodynamic Control when Assessing Mechanisms of Carboxylate-Assisted C–H ActivationThe progression of chiral anions from concepts to applications in asymmetric catalysisRhodium(III)‐Catalyzed Amidation of Unactivated C(sp<sup>3</sup>)H BondsChiral Cyclopentadienyl Ligands: Design, Syntheses, and Applications in Asymmetric CatalysisFull Selectivity Control in Cobalt(III)‐Catalyzed C−H Alkylations by Switching of the C−H Activation MechanismCatalytic Enantioselective Transformations Involving C–H Bond Cleavage by Transition-Metal ComplexesCommunication to the Editor : Synthesis of Fluorine-Containing 6-Arylpurine Derivatives via Cp*Co(Ⅲ)-Catalyzed C-H Bond ActivationAward Accounts : The Chemical Society of Japan Award for Young Chemists for 2013 : Development of Cobalt-Catalyzed C-H Bond Functionalization ReactionsRecent advances in enantioselective direct C-H addition to carbonyls and Michael acceptorsStrategy for catalytic oxidative C-H functionalization : efficient combination of transition-metal catalyst and electrochemical oxidationC-H activation catalyzed by Earth-abundant metals
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- 国立情報学研究所 : CiNii Research
- 提供元機関・データベース
- 雑誌記事索引データベースCrossref科学研究費助成事業データベースCrossrefCrossref
- 書誌ID（NDLBibID）
- 12686449