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Refinado por: Nome da Publicação: Angewandte Chemie International Edition remover assunto: Oxidation remover
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1
An Electron‐Deficient CpE Iridium(III) Catalyst: Synthesis, Characterization, and Application to Ether‐Directed C−H Amidation
An Electron‐Deficient CpE Iridium(III) Catalyst: Synthesis, Characterization, and Application to Ether‐Directed C−H Amidation
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An Electron‐Deficient CpE Iridium(III) Catalyst: Synthesis, Characterization, and Application to Ether‐Directed C−H Amidation

Tomita, Eiki ; Kojima, Masahiro ; Nagashima, Yuki ; Tanaka, Ken ; Sugiyama, Haruki ; Segawa, Yasutomo ; Furukawa, Atsushi ; Maenaka, Katsumi ; Maeda, Satoshi ; Yoshino, Tatsuhiko ; Matsunaga, Shigeki

Angewandte Chemie International Edition, 2023-05, Vol.62 (21), p.e202301259-n/a [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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2
Rhodium(III)-Catalyzed ortho-Heteroarylation of Phenols through Internal Oxidative CH Activation: Rapid Screening of Single-Molecular White-Light-Emitting Materials
Rhodium(III)-Catalyzed ortho-Heteroarylation of Phenols through Internal Oxidative CH Activation: Rapid Screening of Single-Molecular White-Light-Emitting Materials
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Rhodium(III)-Catalyzed ortho-Heteroarylation of Phenols through Internal Oxidative CH Activation: Rapid Screening of Single-Molecular White-Light-Emitting Materials

Li, Bijin ; Lan, Jingbo ; Wu, Di ; You, Jingsong

Angewandte Chemie (International ed.), 2015-11, Vol.54 (47), p.14008-14012 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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3
Ligand‐controlled Regiodivergent C−H Alkenylation of Pyrazoles and its Application to the Synthesis of Indazoles
Ligand‐controlled Regiodivergent C−H Alkenylation of Pyrazoles and its Application to the Synthesis of Indazoles
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Ligand‐controlled Regiodivergent C−H Alkenylation of Pyrazoles and its Application to the Synthesis of Indazoles

Kim, Hyun Tae ; Ha, Hyeri ; Kang, Geunhee ; Kim, Og Soon ; Ryu, Ho ; Biswas, Abul Kalam ; Lim, Sang Min ; Baik, Mu‐Hyun ; Joo, Jung Min

Angewandte Chemie International Edition, 2017-12, Vol.56 (51), p.16262-16266 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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4
Ruthenium Oxidase Catalysis for Site-Selective C-H Alkenylations with Ambient O2 as the Sole Oxidant
Ruthenium Oxidase Catalysis for Site-Selective C-H Alkenylations with Ambient O2 as the Sole Oxidant
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Ruthenium Oxidase Catalysis for Site-Selective C-H Alkenylations with Ambient O2 as the Sole Oxidant

Bechtoldt, Alexander ; Tirler, Carina ; Raghuvanshi, Keshav ; Warratz, Svenja ; Kornhaaß, Christoph ; Ackermann, Lutz

Angewandte Chemie (International ed.), 2016-01, Vol.55 (1), p.264-267 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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5
Molecular Engineering of Chalcogen‐Embedded Anthanthrenes via peri‐Selective C−H Activation: Fine‐Tuning of Crystal Packing for Organic Field‐Effect Transistors
Molecular Engineering of Chalcogen‐Embedded Anthanthrenes via peri‐Selective C−H Activation: Fine‐Tuning of Crystal Packing for Organic Field‐Effect Transistors
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Molecular Engineering of Chalcogen‐Embedded Anthanthrenes via peri‐Selective C−H Activation: Fine‐Tuning of Crystal Packing for Organic Field‐Effect Transistors

Liu, Zheng ; Han, Weiguo ; Lan, Jingbo ; Sun, Lingyan ; Tang, Junbin ; Zhang, Cheng ; You, Jingsong

Angewandte Chemie International Edition, 2023-01, Vol.62 (3), p.e202211412-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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6
Iridium(III) Catalysts with an Amide‐Pendant Cyclopentadienyl Ligand: Double Aromatic Homologation Reactions of Benzamides by Fourfold C−H Activation
Iridium(III) Catalysts with an Amide‐Pendant Cyclopentadienyl Ligand: Double Aromatic Homologation Reactions of Benzamides by Fourfold C−H Activation
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Iridium(III) Catalysts with an Amide‐Pendant Cyclopentadienyl Ligand: Double Aromatic Homologation Reactions of Benzamides by Fourfold C−H Activation

Tomita, Eiki ; Yamada, Kodai ; Shibata, Yu ; Tanaka, Ken ; Kojima, Masahiro ; Yoshino, Tatsuhiko ; Matsunaga, Shigeki

Angewandte Chemie International Edition, 2020-06, Vol.59 (26), p.10474-10478 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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7
Metal-Free Dehydrogenative Diels-Alder Reactions of 2-Methyl-3-Alkylindoles with Dienophiles: Rapid Access to Tetrahydrocarbazoles, Carbazoles, and Heteroacenes
Metal-Free Dehydrogenative Diels-Alder Reactions of 2-Methyl-3-Alkylindoles with Dienophiles: Rapid Access to Tetrahydrocarbazoles, Carbazoles, and Heteroacenes
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Metal-Free Dehydrogenative Diels-Alder Reactions of 2-Methyl-3-Alkylindoles with Dienophiles: Rapid Access to Tetrahydrocarbazoles, Carbazoles, and Heteroacenes

Zhou, Liejin ; Xu, Bing ; Zhang, Junliang

Angewandte Chemie (International ed.), 2015-07, Vol.54 (31), p.9092-9096 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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8
Borylenes: An Emerging Class of Compounds
Borylenes: An Emerging Class of Compounds
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Borylenes: An Emerging Class of Compounds

Soleilhavoup, Michele ; Bertrand, Guy

Angewandte Chemie (International ed.), 2017-08, Vol.56 (35), p.10282-10292 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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9
Phosphine-Stabilized Borylenes and Boryl Anions as Ligands? Redox Reactivity in Boron-Based Pincer Complexes
Phosphine-Stabilized Borylenes and Boryl Anions as Ligands? Redox Reactivity in Boron-Based Pincer Complexes
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Phosphine-Stabilized Borylenes and Boryl Anions as Ligands? Redox Reactivity in Boron-Based Pincer Complexes

Vondung, Lisa ; Frank, Nicolas ; Fritz, Maximilian ; Alig, Lukas ; Langer, Robert

Angewandte Chemie (International ed.), 2016-11, Vol.55 (46), p.14450-14454 [Periódico revisado por pares]

Germany: Blackwell Publishing Ltd

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10
Transition-Metal-Free Synthesis of Carbazoles and Indoles by an SNAr-Based "Aromatic Metamorphosis" of Thiaarenes
Transition-Metal-Free Synthesis of Carbazoles and Indoles by an SNAr-Based "Aromatic Metamorphosis" of Thiaarenes
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Transition-Metal-Free Synthesis of Carbazoles and Indoles by an SNAr-Based "Aromatic Metamorphosis" of Thiaarenes

Bhanuchandra, M. ; Murakami, Kei ; Vasu, Dhananjayan ; Yorimitsu, Hideki ; Osuka, Atsuhiro

Angewandte Chemie (International ed.), 2015-08, Vol.54 (35), p.10234-10238 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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