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Ultrafast Decarboxylation of Organic Peroxides in Solution: Interplay of Different Spectroscopic Techniques, Quantum Chemistry, and Theoretical Modeling
Ultrafast Decarboxylation of Organic Peroxides in Solution: Interplay of Different Spectroscopic Techniques, Quantum Chemistry, and Theoretical Modeling
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Ultrafast Decarboxylation of Organic Peroxides in Solution: Interplay of Different Spectroscopic Techniques, Quantum Chemistry, and Theoretical Modeling

Abel, Bernd ; Aßmann, Jens ; Buback, Michael ; Kling, Matthias ; Schmatz, Stefan ; Schroeder, Jörg

Angewandte Chemie (International ed.), 2003-01, Vol.42 (3), p.299-303 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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2
Ultraschnelle Decarboxylierung organischer Peroxide in Lösung: Zusammenspiel unterschiedlicher spektroskopischer Techniken, Quantenchemie und theoretischer Modellierung
Ultraschnelle Decarboxylierung organischer Peroxide in Lösung: Zusammenspiel unterschiedlicher spektroskopischer Techniken, Quantenchemie und theoretischer Modellierung
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Ultraschnelle Decarboxylierung organischer Peroxide in Lösung: Zusammenspiel unterschiedlicher spektroskopischer Techniken, Quantenchemie und theoretischer Modellierung

Abel, Bernd ; Aßmann, Jens ; Buback, Michael ; Kling, Matthias ; Schmatz, Stefan ; Schroeder, Jörg

Angewandte Chemie, 2003-01, Vol.115 (3), p.311-315 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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3
Ultraschnelle Decarboxylierung organischer Peroxide in Lösung: Zusammenspiel unterschiedlicher spektroskopischer Techniken, Quantenchemie und theoretischer Modellierung
Ultraschnelle Decarboxylierung organischer Peroxide in Lösung: Zusammenspiel unterschiedlicher spektroskopischer Techniken, Quantenchemie und theoretischer Modellierung
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Ultraschnelle Decarboxylierung organischer Peroxide in Lösung: Zusammenspiel unterschiedlicher spektroskopischer Techniken, Quantenchemie und theoretischer Modellierung

Abel, Bernd ; Aßmann, Jens ; Buback, Michael ; Kling, Matthias ; Schmatz, Stefan ; Schroeder, Jörg

Angewandte Chemie, 2003-01, Vol.115 (3), p.311-315 [Periódico revisado por pares]

Weinheim: WILEY‐VCH Verlag

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4
Total Synthesis of (±)-γ-Rubromycin on the Basis of Two Aromatic Pummerer-Type Reactions
Total Synthesis of (±)-γ-Rubromycin on the Basis of Two Aromatic Pummerer-Type Reactions
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Total Synthesis of (±)-γ-Rubromycin on the Basis of Two Aromatic Pummerer-Type Reactions

Akai, Shuji ; Kakiguchi, Keisuke ; Nakamura, Yuka ; Kuriwaki, Ikumi ; Dohi, Toshifumi ; Harada, Shusaku ; Kubo, Ozora ; Morita, Nobuyoshi ; Kita, Yasuyuki

Angewandte Chemie, 2007-10, Vol.119 (39), p.7602-7605 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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5
Total Synthesis of (±)-γ-Rubromycin on the Basis of Two Aromatic Pummerer-Type Reactions
Total Synthesis of (±)-γ-Rubromycin on the Basis of Two Aromatic Pummerer-Type Reactions
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Total Synthesis of (±)-γ-Rubromycin on the Basis of Two Aromatic Pummerer-Type Reactions

Akai, Shuji ; Kakiguchi, Keisuke ; Nakamura, Yuka ; Kuriwaki, Ikumi ; Dohi, Toshifumi ; Harada, Shusaku ; Kubo, Ozora ; Morita, Nobuyoshi ; Kita, Yasuyuki

Angewandte Chemie (International ed.), 2007-01, Vol.46 (39), p.7458-7461 [Periódico revisado por pares]

Weinheim: Wiley-VCH Verlag

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6
Reactivity of a Tetra(o‐tolyl)diborane(4) Dianion as a Diarylboryl Anion Equivalent
Reactivity of a Tetra(o‐tolyl)diborane(4) Dianion as a Diarylboryl Anion Equivalent
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Reactivity of a Tetra(o‐tolyl)diborane(4) Dianion as a Diarylboryl Anion Equivalent

Akiyama, Seiji ; Yamada, Kaito ; Yamashita, Makoto

Angewandte Chemie International Edition, 2019-08, Vol.58 (34), p.11806-11810 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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7
Reactivity of a Tetra(o‐tolyl)diborane(4) Dianion as a Diarylboryl Anion Equivalent
Reactivity of a Tetra(o‐tolyl)diborane(4) Dianion as a Diarylboryl Anion Equivalent
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Reactivity of a Tetra(o‐tolyl)diborane(4) Dianion as a Diarylboryl Anion Equivalent

Akiyama, Seiji ; Yamada, Kaito ; Yamashita, Makoto

Angewandte Chemie, 2019-08, Vol.131 (34), p.11932-11936 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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8
Semihydrogenation of Acetylene on Indium Oxide: Proposed Single‐Ensemble Catalysis
Semihydrogenation of Acetylene on Indium Oxide: Proposed Single‐Ensemble Catalysis
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Semihydrogenation of Acetylene on Indium Oxide: Proposed Single‐Ensemble Catalysis

Albani, Davide ; Capdevila‐Cortada, Marçal ; Vilé, Gianvito ; Mitchell, Sharon ; Martin, Oliver ; López, Núria ; Pérez‐Ramírez, Javier

Angewandte Chemie, 2017-08, Vol.129 (36), p.10895-10900 [Periódico revisado por pares]

Weinheim: Wiley Subscription Services, Inc

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9
Semihydrogenation of Acetylene on Indium Oxide: Proposed Single‐Ensemble Catalysis
Semihydrogenation of Acetylene on Indium Oxide: Proposed Single‐Ensemble Catalysis
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Semihydrogenation of Acetylene on Indium Oxide: Proposed Single‐Ensemble Catalysis

Albani, Davide ; Capdevila‐Cortada, Marçal ; Vilé, Gianvito ; Mitchell, Sharon ; Martin, Oliver ; López, Núria ; Pérez‐Ramírez, Javier

Angewandte Chemie (International ed.), 2017-08, Vol.56 (36), p.10755-10760 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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10
Properties of Sizeable [n]Cycloparaphenylenes as Molecular Models of Single-Wall Carbon Nanotubes Elucidated by Raman Spectroscopy: Structural and Electron-Transfer Responses under Mechanical Stress
Properties of Sizeable [n]Cycloparaphenylenes as Molecular Models of Single-Wall Carbon Nanotubes Elucidated by Raman Spectroscopy: Structural and Electron-Transfer Responses under Mechanical Stress
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Properties of Sizeable [n]Cycloparaphenylenes as Molecular Models of Single-Wall Carbon Nanotubes Elucidated by Raman Spectroscopy: Structural and Electron-Transfer Responses under Mechanical Stress

Alvarez, Miriam Peña ; Burrezo, Paula Mayorga ; Kertesz, Miklos ; Iwamoto, Takahiro ; Yamago, Shigeru ; Xia, Jianlong ; Jasti, Ramesh ; Navarrete, Juan T. López ; Taravillo, Mercedes ; Baonza, Valentín G. ; Casado, Juan

Angewandte Chemie, 2014-07, Vol.126 (27), p.7153-7157 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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