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Activating a [FeFe] Hydrogenase Mimic for Hydrogen Evolution under Visible Light
Activating a [FeFe] Hydrogenase Mimic for Hydrogen Evolution under Visible Light
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Activating a [FeFe] Hydrogenase Mimic for Hydrogen Evolution under Visible Light

Buday, Philipp ; Kasahara, Chizuru ; Hofmeister, Elisabeth ; Kowalczyk, Daniel ; Farh, Micheal K. ; Riediger, Saskia ; Schulz, Martin ; Wächtler, Maria ; Furukawa, Shunsuke ; Saito, Masaichi ; Ziegenbalg, Dirk ; Gräfe, Stefanie ; Bäuerle, Peter ; Kupfer, Stephan ; Dietzek‐Ivanšić, Benjamin ; Weigand, Wolfgang

Angewandte Chemie (International ed.), 2022-05, Vol.61 (20), p.e202202079-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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12
Cobalt(I)-Catalyzed Asymmetric [2+2+2] Cycloaddition of Alkynes and Nitriles: Synthesis of Enantiomerically Enriched Atropoisomers of 2-Arylpyridines
Cobalt(I)-Catalyzed Asymmetric [2+2+2] Cycloaddition of Alkynes and Nitriles: Synthesis of Enantiomerically Enriched Atropoisomers of 2-Arylpyridines
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Cobalt(I)-Catalyzed Asymmetric [2+2+2] Cycloaddition of Alkynes and Nitriles: Synthesis of Enantiomerically Enriched Atropoisomers of 2-Arylpyridines

Gutnov, Andrey ; Heller, Barbara ; Fischer, Christine ; Drexler, Hans-Joachim ; Spannenberg, Anke ; Sundermann, Bernd ; Sundermann, Corinna

Angewandte Chemie (International ed.), 2004-07, Vol.43 (29), p.3795-3797 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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13
Cyclization-Carbonylation-Cyclization Coupling Reactions of Propargyl Acetates and Amides with Palladium(II)-Bisoxazoline Catalysts
Cyclization-Carbonylation-Cyclization Coupling Reactions of Propargyl Acetates and Amides with Palladium(II)-Bisoxazoline Catalysts
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Cyclization-Carbonylation-Cyclization Coupling Reactions of Propargyl Acetates and Amides with Palladium(II)-Bisoxazoline Catalysts

Yasuhara, Sumie ; Sasa, Makiko ; Kusakabe, Taichi ; Takayama, Hiroyuki ; Kimura, Masayuki ; Mochida, Tomoyuki ; Kato, Keisuke

Angewandte Chemie, 2011-04, Vol.123 (17), p.3998-4001 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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14
Facile Chemoenzymatic Strategies for the Synthesis and Utilization of S-Adenosyl-L-Methionine Analogues
Facile Chemoenzymatic Strategies for the Synthesis and Utilization of S-Adenosyl-L-Methionine Analogues
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Facile Chemoenzymatic Strategies for the Synthesis and Utilization of S-Adenosyl-L-Methionine Analogues

Singh, Shanteri ; Zhang, Jianjun ; Huber, Tyler D. ; Sunkara, Manjula ; Hurley, Katherine ; Goff, Randal D. ; Wang, Guojun ; Zhang, Wen ; Liu, Chunming ; Rohr, Jürgen ; Van Lanen, Steven G. ; Morris, Andrew J. ; Thorson, Jon S.

Angewandte Chemie (International ed.), 2014-04, Vol.53 (15), p.3965-3969 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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15
Synthesis, Structure, and Reactivity of Acid‐Free Neutral Oxoborane
Synthesis, Structure, and Reactivity of Acid‐Free Neutral Oxoborane
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Synthesis, Structure, and Reactivity of Acid‐Free Neutral Oxoborane

Wang, Hanqiang ; Zhang, Jie ; Yang, Jingting ; Xie, Zuowei

Angewandte Chemie, 2021-08, Vol.133 (35), p.19156-19160 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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16
Dithiol Proteins as Guardians of the Intracellular Redox Milieu in Parasites: Old and New Drug Targets in Trypanosomes and Malaria-Causing Plasmodia
Dithiol Proteins as Guardians of the Intracellular Redox Milieu in Parasites: Old and New Drug Targets in Trypanosomes and Malaria-Causing Plasmodia
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Dithiol Proteins as Guardians of the Intracellular Redox Milieu in Parasites: Old and New Drug Targets in Trypanosomes and Malaria-Causing Plasmodia

Krauth-Siegel, R. Luise ; Bauer, Holger ; Schirmer, R. Heiner

Angewandte Chemie (International ed.), 2005-01, Vol.44 (5), p.690-715 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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17
Reactivity of ortho-Palladated Phenol Derivatives with Unsaturated Molecules: Insertion of Nitriles into a Late-Transition-Metal-Carbon Bond
Reactivity of ortho-Palladated Phenol Derivatives with Unsaturated Molecules: Insertion of Nitriles into a Late-Transition-Metal-Carbon Bond
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Reactivity of ortho-Palladated Phenol Derivatives with Unsaturated Molecules: Insertion of Nitriles into a Late-Transition-Metal-Carbon Bond

Vicente, José ; Abad, José Antonio ; López-Sáez, María-José ; Jones, Peter G.

Angewandte Chemie (International ed.), 2005-09, Vol.44 (37), p.6001-6004 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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18
Facile Chemoenzymatic Strategies for the Synthesis and Utilization of S-Adenosyl-L-Methionine Analogues
Facile Chemoenzymatic Strategies for the Synthesis and Utilization of S-Adenosyl-L-Methionine Analogues
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Facile Chemoenzymatic Strategies for the Synthesis and Utilization of S-Adenosyl-L-Methionine Analogues

Singh, Shanteri ; Zhang, Jianjun ; Huber, Tyler D. ; Sunkara, Manjula ; Hurley, Katherine ; Goff, Randal D. ; Wang, Guojun ; Zhang, Wen ; Liu, Chunming ; Rohr, Jürgen ; Van Lanen, Steven G. ; Morris, Andrew J. ; Thorson, Jon S.

Angewandte Chemie, 2014-04, Vol.126 (15), p.4046-4050 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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19
Oxidative Carbonylation Reactions: Organometallic Compounds (RM) or Hydrocarbons (RH) as Nucleophiles
Oxidative Carbonylation Reactions: Organometallic Compounds (RM) or Hydrocarbons (RH) as Nucleophiles
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Oxidative Carbonylation Reactions: Organometallic Compounds (RM) or Hydrocarbons (RH) as Nucleophiles

Liu, Qiang ; Zhang, Hua ; Lei, Aiwen

Angewandte Chemie (International ed.), 2011-11, Vol.50 (46), p.10788-10799 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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20
Reactivity of ortho-Palladated Phenol Derivatives with Unsaturated Molecules: Insertion of Nitriles into a Late-Transition-Metal-Carbon Bond
Reactivity of ortho-Palladated Phenol Derivatives with Unsaturated Molecules: Insertion of Nitriles into a Late-Transition-Metal-Carbon Bond
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Reactivity of ortho-Palladated Phenol Derivatives with Unsaturated Molecules: Insertion of Nitriles into a Late-Transition-Metal-Carbon Bond

Vicente, José ; Abad, José Antonio ; López-Sáez, María-José ; Jones, Peter G.

Angewandte Chemie, 2005-09, Vol.117 (37), p.6155-6158 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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