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Refinado por: Nome da Publicação: Angewandte Chemie remover
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1
Traceless Tosylhydrazone-Based Triazole Formation: A Metal-Free Alternative to Strain-Promoted Azide-Alkyne Cycloaddition
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Traceless Tosylhydrazone-Based Triazole Formation: A Metal-Free Alternative to Strain-Promoted Azide-Alkyne Cycloaddition

van Berkel, Sander S. ; Brauch, Sebastian ; Gabriel, Lars ; Henze, Michael ; Stark, Sebastian ; Vasilev, Dimitar ; Wessjohann, Ludger A. ; Abbas, Muhammad ; Westermann, Bernhard

Angewandte Chemie (International ed.), 2012-05, Vol.51 (22), p.5343-5346 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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2
Acyl Fluorides in Late‐Transition‐Metal Catalysis
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Acyl Fluorides in Late‐Transition‐Metal Catalysis

Ogiwara, Yohei ; Sakai, Norio

Angewandte Chemie (International ed.), 2020-01, Vol.59 (2), p.574-594 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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3
A Pure‐Red Doublet Emission with 90 % Quantum Yield: Stable, Colorless, Iodinated Triphenylmethane Solid
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A Pure‐Red Doublet Emission with 90 % Quantum Yield: Stable, Colorless, Iodinated Triphenylmethane Solid

Liu, Cheng‐Hao ; Hamzehpoor, Ehsan ; Sakai‐Otsuka, Yoko ; Jadhav, Thaksen ; Perepichka, Dmitrii F.

Angewandte Chemie (International ed.), 2020-12, Vol.59 (51), p.23030-23034 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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4
“Spurlose” Tosylhydrazon‐basierte Triazolsynthese: eine metallfreie Alternative zur ringspannungskatalysierten Azid‐Alkin‐ Cycloaddition
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“Spurlose” Tosylhydrazon‐basierte Triazolsynthese: eine metallfreie Alternative zur ringspannungskatalysierten Azid‐Alkin‐ Cycloaddition

van Berkel, Sander S. ; Brauch, Sebastian ; Gabriel, Lars ; Henze, Michael ; Stark, Sebastian ; Vasilev, Dimitar ; Wessjohann, Ludger A. ; Abbas, Muhammad ; Westermann, Bernhard

Angewandte Chemie, 2012-05, Vol.124 (22), p.5437-5441 [Periódico revisado por pares]

Weinheim: WILEY‐VCH Verlag

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5
"Spurlose" Tosylhydrazon-basierte Triazolsynthese: eine metallfreie Alternative zur ringspannungskatalysierten Azid-Alkin- Cycloaddition
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Artigo
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"Spurlose" Tosylhydrazon-basierte Triazolsynthese: eine metallfreie Alternative zur ringspannungskatalysierten Azid-Alkin- Cycloaddition

van Berkel, Sander S. ; Brauch, Sebastian ; Gabriel, Lars ; Henze, Michael ; Stark, Sebastian ; Vasilev, Dimitar ; Wessjohann, Ludger A. ; Abbas, Muhammad ; Westermann, Bernhard

Angewandte Chemie, 2012-05, Vol.124 (22), p.5437-5441 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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6
Reductive Amination/Cyclization of Keto Acids Using a Hydrosilane for Selective Production of Lactams versus Cyclic Amines by Switching of the Indium Catalyst
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Reductive Amination/Cyclization of Keto Acids Using a Hydrosilane for Selective Production of Lactams versus Cyclic Amines by Switching of the Indium Catalyst

Ogiwara, Yohei ; Uchiyama, Takuya ; Sakai, Norio

Angewandte Chemie (International ed.), 2016-01, Vol.55 (5), p.1864-1867 [Periódico revisado por pares]

Germany: Blackwell Publishing Ltd

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7
Colossal Negative Thermal Expansion in Electron‐Doped PbVO3 Perovskites
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Colossal Negative Thermal Expansion in Electron‐Doped PbVO3 Perovskites

Yamamoto, Hajime ; Imai, Takashi ; Sakai, Yuki ; Azuma, Masaki

Angewandte Chemie (International ed.), 2018-07, Vol.57 (27), p.8170-8173 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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8
Near‐Infrared Light‐Driven Hydrogen Evolution from Water Using a Polypyridyl Triruthenium Photosensitizer
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Near‐Infrared Light‐Driven Hydrogen Evolution from Water Using a Polypyridyl Triruthenium Photosensitizer

Tsuji, Yutaro ; Yamamoto, Keiya ; Yamauchi, Kosei ; Sakai, Ken

Angewandte Chemie (International ed.), 2018-01, Vol.57 (1), p.208-212 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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9
A Nickel Dithiolate Water Reduction Catalyst Providing Ligand‐Based Proton‐Coupled Electron‐Transfer Pathways
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A Nickel Dithiolate Water Reduction Catalyst Providing Ligand‐Based Proton‐Coupled Electron‐Transfer Pathways

Koshiba, Keita ; Yamauchi, Kosei ; Sakai, Ken

Angewandte Chemie (International ed.), 2017-04, Vol.56 (15), p.4247-4251 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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10
Alcohols as Alkylating Agents: Photoredox‐Catalyzed Conjugate Alkylation via In Situ Deoxygenation
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Alcohols as Alkylating Agents: Photoredox‐Catalyzed Conjugate Alkylation via In Situ Deoxygenation

Wang, Johnny Z. ; Sakai, Holt A. ; MacMillan, David W. C.

Angewandte Chemie (International ed.), 2022-08, Vol.61 (35), p.e202207150-n/a [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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