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1
Tungsten-Based Catalysts for Selective Deoxygenation
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Tungsten-Based Catalysts for Selective Deoxygenation

Angewandte Chemie (International ed.), 2013-05, Vol.52 (19), p.5089-5092 [Peer Reviewed Journal]

Copyright © 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;Copyright Wiley Subscription Services, Inc. May 2013 ;Wageningen University & Research ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201209809 ;PMID: 23554125 ;CODEN: ACIEAY

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2
Ultrarotspektroskopie als analytisches Hilfsmittel
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Ultrarotspektroskopie als analytisches Hilfsmittel

Angewandte Chemie, 1951-09, Vol.63 (17‐18), p.402-411 [Peer Reviewed Journal]

Copyright © 1951 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 0044-8249 ;EISSN: 1521-3757 ;DOI: 10.1002/ange.19510631704

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3
Theoretical Considerations on the Electroreduction of CO to C 2 Species on Cu(100) Electrodes
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Theoretical Considerations on the Electroreduction of CO to C 2 Species on Cu(100) Electrodes

Angewandte Chemie International Edition, 2013-07, Vol.52 (28), p.7282-7285 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201301470

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4
Nature‐Inspired Environmental “Phosphorylation” Boosts Photocatalytic H 2 Production over Carbon Nitride Nanosheets under Visible‐Light Irradiation
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Nature‐Inspired Environmental “Phosphorylation” Boosts Photocatalytic H 2 Production over Carbon Nitride Nanosheets under Visible‐Light Irradiation

Angewandte Chemie International Edition, 2015-11, Vol.54 (46), p.13561-13565 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201505802

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5
Visible‐Light‐Mediated Decarboxylation/Oxidative Amidation of α‐Keto Acids with Amines under Mild Reaction Conditions Using O 2
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Visible‐Light‐Mediated Decarboxylation/Oxidative Amidation of α‐Keto Acids with Amines under Mild Reaction Conditions Using O 2

Angewandte Chemie International Edition, 2014-01, Vol.53 (2), p.502-506 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201308614

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6
Ruthenium(II)‐Catalyzed CH Activation/Alkyne Annulation by Weak Coordination with O 2 as the Sole Oxidant
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Ruthenium(II)‐Catalyzed CH Activation/Alkyne Annulation by Weak Coordination with O 2 as the Sole Oxidant

Angewandte Chemie International Edition, 2015-04, Vol.54 (18), p.5513-5517 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201500600

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7
A Cationic High‐Valent CpCo III Complex for the Catalytic Generation of Nucleophilic Organometallic Species: Directed CH Bond Activation
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A Cationic High‐Valent CpCo III Complex for the Catalytic Generation of Nucleophilic Organometallic Species: Directed CH Bond Activation

Angewandte Chemie International Edition, 2013-02, Vol.52 (8), p.2207-2211 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201209226

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8
Phosphorus‐Doped Graphite Layers with High Electrocatalytic Activity for the O 2 Reduction in an Alkaline Medium
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Phosphorus‐Doped Graphite Layers with High Electrocatalytic Activity for the O 2 Reduction in an Alkaline Medium

Angewandte Chemie International Edition, 2011-03, Vol.50 (14), p.3257-3261 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201006768

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9
Directed Amination of Non-Acidic Arene CH Bonds by a Copper-Silver Catalytic System
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Directed Amination of Non-Acidic Arene CH Bonds by a Copper-Silver Catalytic System

Angewandte Chemie (International ed.), 2013-06, Vol.52 (23), p.6043 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201300135 ;CODEN: ACIEAY

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10
Slow Magnetic Relaxation in a Co II –Y III Single‐Ion Magnet with Positive Axial Zero‐Field Splitting
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Slow Magnetic Relaxation in a Co II –Y III Single‐Ion Magnet with Positive Axial Zero‐Field Splitting

Angewandte Chemie International Edition, 2013-08, Vol.52 (35), p.9130-9134 [Peer Reviewed Journal]

Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201304386

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11
Cyanoalkylation: Alkylnitriles in Catalytic CC Bond-Forming Reactions
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Cyanoalkylation: Alkylnitriles in Catalytic CC Bond-Forming Reactions

Angewandte Chemie (International ed.), 2015-11, Vol.54 (45), p.13170 [Peer Reviewed Journal]

2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim ;ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201502493 ;CODEN: ACIEAY

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12
Metal-Free Radical Azidoarylation of Alkenes: Rapid Access to Oxindoles by Cascade CN and CC Bond-Forming Reactions
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Metal-Free Radical Azidoarylation of Alkenes: Rapid Access to Oxindoles by Cascade CN and CC Bond-Forming Reactions

Angewandte Chemie (International ed.), 2013-07, Vol.52 (31), p.7985 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201303550 ;CODEN: ACIEAY

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13
Single Pyramid Magnets: Dy 5 Pyramids with Slow Magnetic Relaxation to 40 K
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Single Pyramid Magnets: Dy 5 Pyramids with Slow Magnetic Relaxation to 40 K

Angewandte Chemie International Edition, 2011-07, Vol.50 (29), p.6530-6533 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201101932

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14
Selective Methylation of Amines with Carbon Dioxide and H 2
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Selective Methylation of Amines with Carbon Dioxide and H 2

Angewandte Chemie International Edition, 2013-11, Vol.52 (46), p.12156-12160 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201306850

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15
Formation of CSCF3 Bonds through Direct Trifluoromethylthiolation
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Formation of CSCF3 Bonds through Direct Trifluoromethylthiolation

Angewandte Chemie (International ed.), 2013-07, Vol.52 (27), p.6818 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201301438 ;CODEN: ACIEAY

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16
Alkene Trifluoromethylation Coupled with CC Bond Formation: Construction of Trifluoromethylated Carbocycles and Heterocycles
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Alkene Trifluoromethylation Coupled with CC Bond Formation: Construction of Trifluoromethylated Carbocycles and Heterocycles

Angewandte Chemie (International ed.), 2013-04, Vol.52 (14), p.4000 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201210250 ;CODEN: ACIEAY

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17
Size‐Selective Encapsulation of C 60 by [10]Cycloparaphenylene: Formation of the Shortest Fullerene‐Peapod
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Size‐Selective Encapsulation of C 60 by [10]Cycloparaphenylene: Formation of the Shortest Fullerene‐Peapod

Angewandte Chemie International Edition, 2011-08, Vol.50 (36), p.8342-8344 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201102302

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18
Zinc-Catalyzed Alkyne Oxidation/CH Functionalization: Highly Site-Selective Synthesis of Versatile Isoquinolones and [beta]-Carbolines
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Zinc-Catalyzed Alkyne Oxidation/CH Functionalization: Highly Site-Selective Synthesis of Versatile Isoquinolones and [beta]-Carbolines

Angewandte Chemie (International ed.), 2015-07, Vol.54 (28), p.8245 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201502553 ;CODEN: ACIEAY

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19
A Chiral Gold Nanocluster Au 20 Protected by Tetradentate Phosphine Ligands
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A Chiral Gold Nanocluster Au 20 Protected by Tetradentate Phosphine Ligands

Angewandte Chemie International Edition, 2014-03, Vol.53 (11), p.2923-2926 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201308599

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20
Rhodium-Catalyzed Enantioselective Intramolecular CH Silylation for the Syntheses of Planar-Chiral Metallocene Siloles
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Rhodium-Catalyzed Enantioselective Intramolecular CH Silylation for the Syntheses of Planar-Chiral Metallocene Siloles

Angewandte Chemie (International ed.), 2015-06, Vol.54 (23), p.6918 [Peer Reviewed Journal]

ISSN: 1433-7851 ;EISSN: 1521-3773 ;DOI: 10.1002/anie.201502548 ;CODEN: ACIEAY

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