Publikationen - Dr. Kathrin Junge

120.Zhou S, Fleischer S, Jiao H, Junge K, and Beller M. ADVANCED SYNTHESIS & CATALYSIS, 2014, 356, 3451-3455. Cooperative Catalysis with Iron and a Chiral Brønsted Acid for Asymmetric Reductive Amination of Ketones.
119.Werkmeister S, Junge K, Wendt B, Spannenberg A, Jiao H, Bornschein C, Beller M. CHEMISTRY – A EUROPEAN JOURNAL, 2014, 20, 4227-4231. Ruthenium/Imidazolylphosphine Catalysis: Hydrogenation of Aliphatic and Aromatic Nitriles to Form Amines.
118.Werkmeister S, Junge K, Wendt B, Alberico E, Jiao H, Baumann W, Junge H, Gallou F, Beller M. ANGEWANDTE CHEMIE INTERNATIONAL EDITION, 2014, 53, 8722-8726. Hydrogenation of Esters to Alcohols with a Well-Defined Iron Complex.
117.Werkmeister S, Junge K, Beller M. ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2014, 18, 289-302. Catalytic Hydrogenation of Carboxylic Acid Esters, Amides, and Nitriles with Homogeneous Catalysts.
116.Vilches-Herrera M, Werkmeister S, Junge K, Boerner A, Beller M. CATALYSIS SCIENCE & TECHNOLOGY, 2014, 4, 629-632. Selective catalytic transfer hydrogenation of nitriles to primary amines using Pd/C.
115.Stemmler T, Westerhaus FA, Surkus A-E, Pohl M-M, Junge K, and Beller M. GREEN CHEMISTRY, 2014, 16, 4535-4540. General and selective reductive amination of carbonyl compounds using a core-shell structured Co3O4/NGr@C catalyst.
114.Stemmler T, Surkus A-E, Pohl M-M, Junge K, and Beller M. CHEMSUSCHEM, 2014, 7, 3012-3016. Iron-Catalyzed Synthesis of Secondary Amines: On the Way to Green Reductive Aminations.
113.Sorribes I, Junge K, Beller M. CHEMISTRY – A EUROPEAN JOURNAL, 2014, 20, 7878-7883. General Catalytic Methylation of Amines with Formic Acid under Mild Reaction Conditions.
112.Sorribes I, Junge K, and Beller M. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136, 14314-14319. Direct Catalytic N-Alkylation of Amines with Carboxylic Acids.
111.Pisiewicz S, Junge K, Beller M. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2014, 2014, 2345-2349. Mild Hydrosilylation of Amides by Platinum N-Heterocyclic Carbene Catalysts.
110.Li Y, Yan T, Junge K, and Beller M. ANGEWANDTE CHEMIE INTERNATIONAL EDITION, 2014, 53, 10476-10480. Catalytic Methylation of C-H Bonds Using CO2 and H2.
109.Junge K, Wendt B, Jiao H, and Beller M. CHEMCATCHEM, 2014, 6, 2810-2814. Iridium-Catalyzed Hydrogenation of Carboxylic Acid Esters.
108.Bornschein C, Werkmeister S, Wendt B, Jiao H, Alberico E, Baumann W, Junge H, Junge K, and Beller M. NATURE COMMUNICATIONS, 2014, 5, 4111. Mild and selective hydrogenation of aromatic and aliphatic (di)nitriles with a well-defined iron pincer complex.
107.Banerjee D, Junge K, Beller M. ORGANIC CHEMISTRY FRONTIERS, 2014, 1, 368-372. Palladium-catalysed regioselective hydroamination of 1,3-dienes: synthesis of allylic amines.
106.Banerjee D, Junge K, and Beller M. ANGEWANDTE CHEMIE INTERNATIONAL EDITION, 2014, 53, 13049-13053. Cooperative Catalysis by Palladium and a Chiral Phosphoric Acid: Enantioselective Amination of Racemic Allylic Alcohols.
105.Banerjee D, Junge K, Beller M. ANGEWANDTE CHEMIE INTERNATIONAL EDITION, 2014, 53, 1630-1635. A General Catalytic Hydroamidation of 1,3-Dienes: Atom-Efficient Synthesis of N-Allyl Heterocycles, Amides, and Sulfonamides.

104.

Banerjee D, Jagadeesh RV, Junge K, Pohl M-M, Radnik J, Brueckner A, Beller M. ANGEWANDTE CHEMIE INTERNATIONAL EDITION, 2014, 53, 4359-4363. Convenient and Mild Epoxidation of Alkenes Using Heterogeneous Cobalt Oxide Catalysts.
103.Wienhoefer G, Westerhaus FA, Junge K, Beller M JOURNAL OF ORGANOMETALLIC CHEMISTRY 2013, 744, 156-159. Fast and Selective Iron-Catalyzed Transfer Hydrogenations of Aldehydes.
102.Bornschein C, Werkmeister S, Junge K, Beller M NEW JOURNAL OF CHEMISTRY 2013, 37, 2061-2065. TBAF-catalyzed hydrosilylation for the reduction of aromatic nitriles.
101.Fleischer S, Zhou S, Werkmeister S, Junge K, Beller M CHEMISTRY – A EUROPEAN JOURNAL 2013, 19, 4997-5003. Cooperative Iron-Bronsted Acid Catalysis: Enantioselective Hydrogenation of Quinoxalines and 2H-1,4-Benzoxazines.
100.Fleischer S, Zhou S, Junge K, Beller M  ANGEWANDTE CHEMIE – INTERNATIONAL EDITION 2013 52 5120-5124. General and Highly Efficient Iron-Catalyzed Hydrogenation of Aldehydes, Ketones, and α,β-Unsaturated Aldehydes.
99.Junge K, Wendt B, Zhou S, Beller M EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2013, 2061-2065. Iron-Catalyzed Reduction of Carboxylic Esters to Alcohols.
98.Kelsen V, Wendt B, Werkmeister S, Junge K, Beller M, Chaudret B CHEMCOMM 2013, 49, 3416-3418. The Use of Ultrasmall Iron(0)Nanoparticles as Catalysts for the Selective Hydrogenation of Unsaturated C-C Bonds.
97.Li Y, Molina de La Torre JA, Grabow K, Bentrup U, Junge K, Zhou S, Brueckner A, Beller M Angewandte Chemie - International Edition 2013, 52, 11577-11580. Selective Reduction of Amides to Amines by Boronic Acid Catalyzed Hydrosilylation.
96.Li Y, Junge K, Beller M CHEMCATCHEM 2013, 5, 1072-1074. Improving the Efficiency of the Hydrogenation of Carbonates and Carbon Dioxide to Methanol.
95.Li Y, Sorribes I, Yan T, Junge K, Beller M ANGEWANDTE CHEMIE - INTERNATIONAL EDITION 2013, 52, 12156-12160. Selective Methylation of Amines with Carbon Dioxide and H2.
94.Li Y, Fang X, Junge K, Beller M ANGEWANDTE CHEMIE – INTERNATIONAL EDITION 2013, 52, 9568-9571. A General Catalytic Methylation of Amines Using Carbon Dioxide.
93.Lu LQ, Li Y, Junge K, Beller M ANGEWANDTE CHEMIE – INTERNATIONAL EDITION  2013, 52, 8382-8386. Iron-Catalyzed Hydrogenation for the In Situ Regeneration of an NAD(P)H Model: Biomimetic Reduction of ....-Keto/...-Iminoesters.
92.Prat I, Font D, Company A, Junge K, Ribas X, Beller M, Costas M ADVANCED SYNTHESIS & CATALYSIS 2013, 355, 947-956. Fe(PyTACN)-Catalyzed cis-Dihydroxylation of Olefins with Hydrogen Peroxide.
91.Werkmeister S, Bornschein C, Junge K, Beller M CHEMISTRY-  A EUROPEAN JOURNAL 2013, 19, 4437-4440. Selective Ruthenium-Catalyzed Transfer Hydrogenations of Nitriles to Amines with 2-Butanol.
90.Werkmeister S, Bornschein C, Junge K, Beller M EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2013, 3671-3674. Ruthenium-Catalyzed Transfer Hydrogenation of Nitriles: Reduction and Subsequent N-Monoalkylation to Secondary Amines.
89.Werkmeister S, Bornschein C, Junge K, Beller M EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2013, 3671-3674. Ruthenium-Catalyzed Transfer Hydrogenation of Nitriles: Reduction and Subsequent N-Monoalkylation to Secondary Amines.
88.Westerhaus FA, Jagadeesh RV, Wienhoefer G, Pohl MM, Radnik J, Surkus AE, Rabeah J, Junge K, Junge H, Nielsen M, Brueckner A, Beller M NATURE CHEMISTRY 2013, 5, 537-543. Heterogenized Cobalt Oxide Catalysts for Nitroarene Reduction by Pyrolysis of Molecularly Defined Complexes.
87.Westerhaus FA, Wendt B, Dumrath A, Wienhoefer G, Junge K, Beller M CHEMSUSCHEM 2013, 6, 1001-1005. Ruthenium Catalysts for Hydrogenation of Aromatic and Aliphatic Esters: Make Use of Bidentate Carbene Ligands.
86.Wienhoefer G, Baseda-Krueger M, Ziebart C, Westerhaus FA, Baumann W, Jackstell R, Junge K, Beller M Chemical Communications 2013, 49, 9089-9091. Hydrogenation of Nitroarenes Using Defined Iron–Phosphine Catalysts.
85.Wienhoefer G, Westerhaus FA, Junge K, Ludwig R, Beller M  CHEMISTRY – A EUROPEAN JOURNAL 2013, 19, 7701-7707. A Molecularly Defined Iron-Catalyst for the Selective Hydrogenation of α,β-Unsaturated Aldehydes.
84.S. Fleischer, S. Zhou, S. Werkmeister, K. Junge, M. Beller, Chem. Eur. J. 2013, DOI: 10.1002/chem.20120436, Cooperative Iron-Brønsted Acid Catalysis: Enantioselective Hydrogenation of Quinoxalines and 2H-1,4-Benzoxazines.
83.K. Kiersch, Y. Li, K. Junge, N. Szesni, R. Fischer, F. E. Kühn, M. Beller, Eur. J. Inorg. Chem. 2012, 36, 5972-5978, Catalytic Epoxidations with Pyridinebisoxazoline-Methyltrioxorhenium Complexes and Nitrogen-Containing Catalyst Systems.
82.Y. Li, L.-Q. Lu, S. Das, S. Pisiewicz, K. Junge, M. Beller, JACS 2012, 134, 18325-18329. Highly Chemoselective Metal-free Reduction of Phosphine Oxides to Phosphines.
81.D. Banerjee, R. V. Jagadeesh, K. Junge, H. Junge, M. Beller, Angew. Chem. 2012, 124, 11724-11728; Angew. Chem. Int. Ed. 2012, 51, 11556-11560, Efficient and Convenient Palladium-catalyzed Amination of Allylic Alcohols with N-Heterocycles. (Hot topic)
80.D. Banerjee, R. V. Jagadeesh, K. Junge, H. Junge, M. Beller, ChemSusChem 2012, 5, 2039-2044; An Efficient and Convenient Palladium Catalyst System for the Synthesis of Amines from Allylic Alcohols.
79.S. Werkmeister, K. Junge, M. Beller, Green Chemistry, 2012, 14, 2371-2374, Copper-catalyzed reductive Amination of Aromatic and Aliphatic Ketones with Anilines using environmental-friendly Molecular Hydrogen.
78.S. Werkmeister, S. Fleischer, K. Junge, M. Beller, Chem. Asian J. 2012, 7, 2562-2568, Towards a zinc-catalyzed asymmetric hydrogenation/transfer hydrogenation of imines to amines.
77.I. Sorribes, G. Wienhöfer, C. Vicent, K. Junge, R. Llusar, M. Beller, Angew. Chem. 2012, 124, 7914-7918; Angew. Chem. Int. Ed. 2012, 51, 7794-7798, Chemoselective Transfer Hydrogenation of Nitroarenes Mediated by Cubane-Type Mo3S4 Cluster Catalysts.
76.S. Das, Y. Li, K. Junge, M. Beller, Chem. Commun. 2012, 48, 10742-10744, Synthesis of Ethers from Esters via Iron-catalyzed Hydrosilylation.
75.K. Junge, B. Wendt, F. A. Westerhaus, A. Spannenberg, H. Jiao, M. Beller, Chem. Eur. J. 2012, 18, 9011-9018; New Phosphine-Imidazolyl Ligands for the efficient Ruthenium catalysed Hydrogenation of Carboxylic Esters.
74.Y. Li, S. Das, S. Zhou, K. Junge, M. Beller, JACS 2012, 134, 9727-9732, General and Selective Copper-catalyzed Reduction of tertiary and secondary Phosphine Oxides: Convenient Synthesis of Phosphines.
73.G. Wienhöfer, F. Westerhaus, R. V. Jagadeesh, K. Junge, H. Junge, M. Beller, Chem. Commun. 2012, 48, 4827-4829; Iron-catalyzed semihydrogenation of terminal alkynes.
72.S. Das, B. Wendt, K. Möller, K. Junge, M. Beller, Angew. Chem. 2012, 124, 1694-1698; Angew. Chem. Int. Ed. 2012, 51, 1662-1666; Two Iron Catalysts are better than one: A General and Convenient Reduction of Aromatic and Aliphatic Primary Amides.
71.S. Werkmeister, S. Fleischer, K. Junge, M. Beller; ChemSusChem 2012, 5, 777-782.; Development of New Hydrogenations of Imines and Benign Reductive Hydroaminations: Zinc Triflate as Catalyst.
70.S. Fleischer, S. Werkmeister, S. Zhou, K. Junge, M. Beller, Chem. Eur. J. 2012, 18, 9005-9010, Consecutive Intermolecular Hydroamination/Asymmetric Hydrogenation: Cooperative Transition Metal and Chiral Brønsted Acid Catalysis.
69.K. Junge, K. Möller, B. Wendt, S. Das, D. Gördes, K. Thurow, M. Beller, Chem. Asian J. 2012, 7, 314-320, Enantioselective Zinc-catalyzed hydrosilylation of ketones using pybox or pybim ligands.
68.S. Das, B. Join, K. Junge, M. Beller, Chem. Commun. 2012, 48, 2683-2685, A General and selective Copper Catalyzed Reduction of Secondary Amides.
67.R. V. Jagadeesh, G. Wienhöfer, F. A. Westerhaus, A.-E. Surkus, H. Junge, K. Junge, M. Beller, Chem. Eur. J. 2011, 51, 14375-14379. A Convenient and General Ruthenium-catalyzed Transfer hydrogenation of Nitro-and Azobenzenes.
66.S. Fleischer, S. Zhou, K. Junge, M. Beller, Chem. Asian J. 2011, 6, 2240-2245. An Easy and General Iron-catalyzed Reductive Amination of Aldehydes and Ketones with Anilines.
65.G. Wienhöfer, I. Sorribes, A. Boddien, F. Westerhaus, K. Junge, H. Junge, R. Llusar, M. Beller, J. Am. Chem. Soc. 2011, 133, 12875–12879. Mild and fast reduction of nitroarenes using well-defined iron catalyst.
64.R. V. Jagadeesh, G. Wienhöfer, F. A. Westerhaus, A.-E. Surkus, M.-M. Pohl, H. Junge, K. Junge, M. Beller, Chem. Commun. 2011, 47, 10972-10974. Efficient and highly selective iron-catalyzed reduction of nitroarenes to anilines.
63.S. Das, D. Addis, L. R. Knöpke, U. Bendrup, K. Junge, A. Brückner, M. Beller, Angew. Chem. 2011; 123, 9346-9359. Angew. Chem. Int. Ed. 2011, 50, 9180-9184; Convenient and chemoselective catalytic monoreductions of phthalimides and imidazolidine-2,4-diones.
62.S. Das, D. Addis, K. Junge, M. Beller; Chem. Eur. J. 2011, 17, 12186-12192. Zinc-catalyzed Chemoselective Reduction of Tertiary and Secondary Amides to Amines. DOI: 10.1002/chem.201101143; 13.9. online
61.B. Join, K. Möller, C. Ziebart, K. Schröder, D. Gördes, K. Thurow, K. Junge, M. Beller, Adv. Syn. Cat. 2011, 353, 3023-3030; Selective iron-catalyzed oxidation of benzylic and allylic alcohols.
60.S. Das, K. Möller, K. Junge, M. Beller, Chem. Eur. J. 2011, 17, 7414-7417. Zn-catalyzed chemoselective reduction of esters to alcohols.
59.D. Addis, S. Das, K. Junge, M. Beller, Angew. Chem. 2011, 123, 6128-6135. Angew. Chem. Int. Ed. 2011, 50, 6004-6011, Selective Reduction of Carboxylic Acid Derivatives by Catalytic Hydrosilylation.
58.S. Zhou, S. Fleischer, K. Junge, and M. Beller, Angew. Chem. Int. Ed. 2011, 50, 5120-5124. Angew. Chem. 2011, 123, 5226-5230, Cooperative Transition Metal and Chiral Brønsted Acid Catalysis: Enantioselective Hydrogenation of Imines to form Amines. (VIP-paper, cover picture May)
57.K. Möller, G. Wienhöfer, F. Westerhaus, K. Junge, M. Beller, Catalysis Today 2011, 173, 68-75. Oxidation of 1,2,4-Trimethylbenzene (TMB), 2,3,6-Trimethylphenol (TMP) and 2-Methylnaphthalene to 2,3,5-Trimethylbenzoquinone (TMBQ) and Menadione (Vitamin K3).
56.S. Gladiali, E. Alberico, K. Junge, M. Beller, Chem. Soc. Reviews 2011, 40, 3744-3763. BINEPINE: a chiral binaphthalene-core monophosphine ligand for multipurpose asymmetric catalysis.
55.K. Möller, K. Junge, A. Spannenberg, M. Beller, Acta Cryst. 2011, E67, o1181. 2,6-Bis((S)-4-benzyl-4,5-dihydrooxazol-2-yl)pyridine.
54.K. Junge, K. Schröder, M. Beller, Chem. Commun. 2011, 47, 4849-4859. Homogeneous catalysis using iron complexes: Recent developments in selective reductions (top 10 most accessed on March).
53.K. Schröder, K. Junge, B. Bitterlich, Top. Organomet. Chem. 2011, 33, 83-109. Fe-Catalyzed Oxidation Reactions of Olefins, Alkanes, and Alcohols: Involvement of Oxo- and Peroxo Complexes.
52.K. Junge, B. Wendt, D. Addis, S. Zhou, S. Das, S. Fleischer, M. Beller; Chem. Eur. J. 2011, 17, 101-105. Copper-catalyzed Enantioselective Hydrogenation of Ketones.
51.K. Schröder, B. Join, A. J. Amali, K. Junge, X. Ribas, M. Costas, M. Beller; Angew. Chem. 2011, 123, 1461-1465. Angew. Chem. Int. Ed. 2011, 50, 1425-1429; A Biomimetic Iron Catalyst for Epoxidation of Olefins with Molecular Oxygen at Room Temperature.
50.D. Addis, S. Zhou, S. Das, K. Junge, J. Harloff, H. Lund, H. Kosslick, A. Schulz, M. Beller; Chem. Asian J. 2010, 5, 2341-2345. Hydrosilylation of Ketones: From Metal Organic Framework to Simple Base Catalysts.
49.S. Enthaler, K. Schröder, S. Inuoe, B. Eckhardt, K. Junge, M. Beller, M. Driess, Eur. J. Org. Chem. 2010, 25, 4893-4901. Formamidines – Versatile Ligands for Zinc-catalyzed Hydrosilylation and Iron-catalyzed Epoxidation Reactions.
48.S. Zhou, S. Fleischer, K. Junge, S. Das, D. Addis, M. Beller, Angew. Chem. 2010, 122, 8298-8302. Angew. Chem. Int. Ed. 2010, 49, 8121-8125; Iron-Catalyzed Asymmetric Transfer Hydrogenation of Imines. (VIP-paper, hot paper; inside cover)
47.K. Möller, G. Wienhöfer, K. Schröder, B. Join, K. Junge, M. Beller, Chem. Eur. J. 2010, 16, 10300-10303. Selective Iron-catalyzed Oxidation of Phenols and Arenes with Hydrogen Peroxide: Synthesis of Vitamin E intermediates and Vitamin K3. (VIP-paper, cover)
46.E. Alberico, S. Gladiali, R. Taras, K. Junge, M. Beller, Tetrahedron: Asymmetry 2010, 21, 1406-1410. Expanding the scope of atropisomeric monodentate P-donor ligands in asymmetric catalysis. Asymmetric allylic alkylation of 1,3-diphenylpropenyl-1-esters by Pd/BINEPINE catalysts.
45.S. Das, S. Zhou, D. Addis, S. Enthaler, K. Junge, M. Beller, Top. Catal. 2010, 53, 979-984. Selective Catalytic Reductions of Amides and Nitriles to Amines.
44.K. Schröder, S. Enthaler, B. Join, K. Junge, M. Beller, Adv. Synth. Cat. 2010; 352, 1771-1778. Iron-catalyzed Epoxidation of Aromatic Olefins and 1,3-Dienes.
43.G. Wienhöfer, K. Schröder, K. Möller, K. Junge, M. Beller, Adv. Synth. Cat. 2010; 352, 1615-1620. A Novel Process for Selective Ruthenium-catalyzed Oxidation of Naphthalenes and Phenols.
42.K. Schröder, K. Junge, A. Spannenberg, M. Beller, Catal. Today 2010, 157, 364-370. Design of a Bio-inspired Imidazole-based Iron Catalyst for Epoxidation of Olefins: Mechanistic Insights.
41.D. Addis, N. Shaikh, S. Zhou, S. Das, K. Junge, M. Beller; Chem. Asian J. 2010, 5, 1687-1691. Chemo- and Stereoselective Iron-catalyzed Hydrosilylation of Ketones.
40.K. Junge, B. Wendt, S. Enthaler, M. Beller, ChemCatChem 2010, 2, 453-458. Palladium-Catalyzed Enantioselective Hydrosilylation of Aromatic Olefins.
39.S. Das, D. Addis, S. Zhou, K. Junge, M. Beller; J. Am. Chem. Soc. 2010, 132, 1770-1771. Zinc-Catalyzed Reduction of Amides: Unprecedented Selectivity and Functional Group Tolerance.
38.K. Junge, B. Wendt, N. Shaikh, M. Beller, Chem. Commun. 2010, 46, 1769-1771. Iron-catalyzed selective reduction of nitroarenes to anilines using organosilanes.
37.K. Junge, B. Wendt, D. Addis, S. Zhou, S. Das, M. Beller, Chem. Eur. J. 2010, 16, 68-73. Copper-Catalyzed Enantioselective Hydrosilylation of Ketones by Using Monodentate Binaphthophosphepine Ligands.
36.S. Zhou, D. Addis, S. Das, K. Junge, M. Beller, Chem. Commun. 2009, 4883-4885; New catalytic properties of iron complexes: dehydration of amides to nitriles.
35.S. Zhou, K. Junge, D. Addis, S. Das, M. Beller, Angew. Chem. 2009, 121, 9671-9674; Angew. Chem. Int. Ed. 2009 48 9507-9510; A Convenient and General Iron-Catalyzed Reduction of Amides to Amines.
34.E. Öchsner, K. Schneiders, K. Junge, M. Beller, P. Wasserscheid, Applied Catalysis A: General 2009, 364, 8-14. Highly enantioselective Ru-catalyzed asymmetric hydrogenation of b-keto ester in ionic liquid/methanol mixtures.
33.

G. Erre, S. Enthaler, K. Junge, D. Addis, M. Beller, Adv.

Synth. Cat. 2009, 351, 1437–1441. Iridium-Catalysed Asymmetric Hydrogenation of Enamides in the Presence of 3,3'-Substituted H8-Phosphoramidites.
32.S. Zhou, K. Junge, D. Addis, S. Das, M. Beller, Org. Lett., 2009, 11, 2461-2464. A General and Convenient Catalytic Synthesis of Nitriles from Amides and Silanes.
31.D. Addis, S. Enthaler, K. Junge, B. Wendt, M. Beller,  Tetrahedron Lett. 2009, 50, 3654–3656. Ruthenium N-heterocyclic carbene catalysts for selective reduction of nitriles to primary amines.
30.K. Schröder, S. Enthaler, B. Bitterlich, T. Schulz, A. Spannenberg, M. K. Tse, K. Junge, M. Beller, Chem. Eur. J. 2009, 15, 5471-5481. Design of and Mechanistic Studies on a Biomimetic Iron–Imidazole Catalyst System for Epoxidation of Olefins with Hydrogen Peroxide.
29.E. Öchsner, B. Etzold, K. Junge, M. Beller, P. Wasserscheid,  Adv. Synth. Cat. 2009, 351, 235-245. Kinetic Study of the Asymmetric Hydrogenation of Methyl Acetoacetate in the Presence of a Ruthenium Binaphthophosphepine Complexe.
28.S. Enthaler, K. Junge,  D. Addis, G. Erre,  M. Beller, ChemSusChem 2008, 1, 1006-1010. A Practical and Benign Synthesis of Primary Amines through Ruthenium-Catalyzed Reduction of Nitriles
27.

S. Enthaler, D. Addis, K. Junge, G. Erre, M. Beller, Chem. Eur. J. 2008, 14, 9491-9494. A General and Environmentally Benign Catalytic Reduction of Nitriles to Primary Amines.

26.

S. Enthaler, G. Erre, K. Junge, D. Addis, R. Kadyrov, M. Beller, Chem. Asian. J. 2008, 3, 1104-1110. Synthesis of Enantiomerically Pure 1,2,3,4-Tetrahydro-β-carbolines and N-Acyl-1-aryl Ethylamines by Rhodium-Catalyzed Hydrogenation.

25.

S. Enthaler, G. Erre, K. Junge, K. Schröder, D. Addis, D. Michalik, M. Hapke, D. Redkin, M. Beller, Eur. J. Org. Chem. 2008, 19, 3352-3362. Iridium-Catalyzed Hydrogenation of ß-Dehydroamino Acid Derivatives Using Monodentate Phosphoramidites.

24.

G. Erre, K. Junge, S. Enthaler, D. Addis, D. Michalik, A. Spannenberg, M. Beller, Chem. Asian. J. 2008, 3, 887-894. Synthesis of Novel Monodentate Phosphoramidites and Their Application in Iridium-Catalyzed Asymmetric Hydrogenation.

23.

G. Erre, S. Enthaler, K. Junge, S. Gladiali, M. Beller, J. Mol. Cat. 2008, 280, 148-155. Novel rhodium catalysts for asymmetric hydroformylation of styren: Study of electronic and steric effects of phosphorus seven-membered ring ligands.

22.

G. Erre, S. Enthaler, K. Junge, S. Gladiali, M. Beller, Coord. Chem. Rev. 2008, 22, 471-491. Synthesis and application of chiral monodentate phosphines in asymmetric hydrogenation.

21.

S. Enthaler, B. Spilker, G. Erre, K. Junge, M. K. Tse, M. Beller, Tetrahedron 2008, 64, 3867-3876. Biomimetic transfer hydrogenation with iron-porpyrin catalysts.

20.

N. S. Shaikh, S. Enthaler, K. Junge, M. Beller, Angew. Chem. Int. Ed. 2008, 47, 2497-2501. Iron-catalyzed Enantioselective Hydrosilylation of Ketones under Mild Conditions.

19.

S. Enthaler, K. Junge, M. Beller, Angew. Chem. Int. Ed. 2008, 47, 3317-3321. Sustainable Metal Catalysis with Iron

– From Rust to a Rising Star?
18.

S. Enthaler, G. Erre, K. Junge, J. Holz, A. Börner, E. Alberico, I. Nieddu, S. Gladiali, M. Beller, Org. Process Res. Dev. 2007, 11, 568-577; Development of Practical Rhodium Phosphine Catalysts for the Hydrogenation of β-Dehydroamino Acid Derivatives.

17.

S. Enthaler, B. Hagemann, S. Bhor, G. Anilkumar, M. K. Tse, B. Bitterlich, K. Junge, G. Erre, M. Beller, Adv. Synth. Cat. 2007, 349, 853-860. New Ruthenium Catalysts for Asymmetric Transfer Hydrogenation of Prochiral Ketons.

16.

S. Enthaler, G. Erre, K. Junge, D. Michalik, A. Spannenberg, F. Marras, S. Gladiali, M. Beller, Tetrahedron: Asymmetry 2007, 18, 1288-1298. Enantioselective rhodium-catalyzed hydrogenation of enol carbamates in the presence of monodentate phosphines.

15.

K. Junge, B. Hagemann, S. Enthaler, G. Erre, M. Beller, ARKIVOC, 2007, (v), 50-66.

14.

N. Shaikh, K. Junge, M. Beller, Org. Lett. 2007, 26, 5429-5432. A Convenient and Generell Iron-Catalyzed Hydrosilylation of Aldehydes.

13.S. Enthaler, R. Jackstell, B. Hagemann, K. Junge, G. Erre, M. Beller, J. Organomet. Chem. 2006, 691, 4652-4659. Efficient Transfer Hydrogenation of Ketones in the Presence of Ruthenium N-heterocyclic carbene catalysts.
12.S. Enthaler, G. Erre, M. K. Tse, K. Junge, M. Beller, Tetrahedron Lett. 2006, 47, 8095-8099. Biomimetic Transfer Hydrogenation of Ketones with Homogeneous Iron Porphyrin Catalysts.
11.S. Enthaler, B. Hagemann, G. Erre, K. Junge, M. Beller, Chem. Asian. J. 2006, 1, 598-604. An Environmentally Benign Process for the Hydrogenation of Ketones with Homogeneous Iron Catalysts.

10.

S. Enthaler, B. Hagemann, K. Junge, G. Erre, M. Beller, Eur. J. Org. Chem.  2006, 2912-2917. Enantioselective Rhodium-Catalyzed Hydrogenation of Enamides in the Presence of Chiral Monodentate Phosphanes.

9.

B. Hagemann, K. Junge, S. Enthaler, M. Michalik, T. Riermeier, A. Monsees, M. Beller, Adv. Synth. Catal.. 2005, 347, 1978-1986. A General Method for the Enantioselective Hydrogenation of β-Keto Esters using Monodentate Binaphthophosphepine Ligands.

8.

K. Junge, B. Hagemann, S. Enthaler, A. Spannenberg, M. Michalik, G. Oehme, A. Monsees, T. Riermeier, M. Beller, Tetrahedron: Asymmetry 2004, 15, 2621-2631. Synthesis of chiral monodentate binaphthophosphepine ligands and their application in asymmetric hydrogenations.

7.

K. Junge, B. Hagemann, S. Enthaler, G. Oehme, M. Michalik; A. Monsees, T. Riermeier, U. Dingerdissen, M. Beller, Angew. Chem. 2004, 116, 5176-5179. Angew. Chem. Int. Ed. 2004, 43, 5066-5069. Enantioselective Hydrogenation of β-Ketoesters with Monodentate Ligands.

6.

K. Junge, G. Oehme, A. Monsees, T. Riermeier, U. Dingerdissen, M. Beller, J. Organomet. Chem. 2003, 675, 91-96. Synthesis of new chiral monodentate aminophosphinites and their use in catalytic asymmetric hydrogenation.

5.

K. Junge, G. Oehme, A. Monsees, T. Riermeier, U. Dingerdissen, M. Beller, Tetrahedron Lett. 2002, 43, 4977-4980. Synthesis of new chiral monodentate phosphines and their use in asymmetric hydrogenation.

4.J. Schneider, E. Popowski, K. Junge, H. Reinke, Z. anorg. allg. Chem. 2001, 627, 2680-2692. Reactions of Lithium Hydridosilylamides RR´(H)Si-N(Li)R´´ with Chlorotrimethylsilane in Tetrahydrofuran and nonpolar solvents: N-Silylation and/or Formation of Cyclodisilazanes.
3.K. Junge, E. Popowski, M. Michalik, Z. anorg. allg. Chem. 1999, 625, 1532-1541. Preparation, Properties, and Reaction Behaviour of 2-[(Dimethylamino)methyl]phenyl- and 8-(Dimethylamino)naphthyl-substituted Lithium Hydridosilylamides. Formation of silanimines by elimination of lithium hydride.
2.K. Junge, E. Popowski, R. Kempe, W. Baumann, Z. anorg. allg. Chem. 1998, 624, 1369-1375. Lithium Hydridosilylamides R2(H)SiN(Li)R´- Preparation, Properties, and Crystal Structures.
1.K. Junge, N. Peulecke, K. Sternberg, H. Reinke, E. Popowski, Organosilicon Chemistry III. From Molecules to Materials 1998, 353-357. Reactions of hydridosilylamides.
10. M. Beller, W. Bonrath, K. Junge, P. McNeice, J. A. Medlock, M.-A. Mueller; New cobald catalyst supported on silica; EP 21164785 (25.03.2021)
9. M. Beller, W. Bonrath, K. Junge, P. McNeice, J. A. Medlock, M.-A. Mueller; New nickel catalyst supported on silica; EP 21164783 (25.03.2021)
8. C. Schotes, M. Beller, K. Junge, W. Liu, J. Schneekönig, T. Leischner; Verbesserte Enantioselektive Hydrierung von 4-substituierten 1,2-Dihydrochinolinen in Gegenwart eines chiralen Iridiumkatalysators und eines Additivs; EP 19199632 (25.09.2019)
7. C. Schotes, M. Beller, K. Junge, W. Liu, J. Schneekönig, T. Leischner; New iridium catalysts for enantioselective hydrogenation of 4-substituted 1,2-dihydroquinolines; EP 19199636 (25.09.2019)
6. M. Checinski, M. Beller, P. Ryabchuk, K. Junge; Process for producing methanol; DE 102018133689 (28.12.2018)
5. S. Bachmann, M. Beller, M. Garbe, K. Junge, M. Scalone; Chiral Metal Complex Compounds; EP 17165855; WO2018189060 (11.04.2017).
4. S. Bachmann, M. Beller, D. Formenti, K. Junge, B. Sahoo, M. Scalone, Ch. Topf; Nitrogen-Containing Biopolymer-Based Catalysts, their preparation and uses in Hydrogenation Processes, Reductive Dehalogenation and Oxidation; EP 16002691 (19.12.2016).
3. G. Wienhöfer, F. Westerhaus, K. Junge, M. Beller, R. Ludwig, 102012212799.2, "Verfahren zur katalytischen Hydrierung von Alhyden", (20.07.2012)
2. F. A. Westerhaus, R. V. Jagadeesh, G. Wienhöfer, A.-E. Surkus, K. Junge, H. Junge, M. Beller, DE 102012209634.5; "Verwendung von thermisch behandelten geträgerten Kobaltkatalysatoren zur Hydrierung von Nitroaromaten" (08.06.2012)
1. Beller, Matthias; Junge, Kathrin; Monsees, Axel; Riermeier, Thomas; Trautwein, Harald; WO 200303350, Degussa AG, "Neue chirale Liganden und deren Übergangsmetallkomplexe sowie deren katalytische Anwendung", DE 10150335 (15.10.2001)