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1. Full Text Catalytic C(sp3)−H Arylation of Free Primary Amines with an exo Directing Group Generated In Situ
by Xu, Yan and Young, Michael C and Wang, Chengpeng and Magness, David M and Dong, Guangbin
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2016, Volume 55, Issue 31, pp. 9084 - 9087
palladium catalysis | C−H activation | directing groups | primary amines | arylation | Aniline | Palladium | Catalysis
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2. Full Text A Hydrazone‐Based exo‐Directing‐Group Strategy for β C−H Oxidation of Aliphatic Amines
by Huang, Zhongxing and Wang, Chengpeng and Dong, Guangbin
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2016, Volume 55, Issue 17, pp. 5299 - 5303
amines | oxidation | palladium | C−H activation | hydrazones | Hydrazones | Oxidation | Palladium | Amines | C-H activation
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3. Full Text Engineering the Active Site of an (S)‐Selective Amine Transaminase for Acceptance of Doubly Bulky Primary Amines
by Land, Henrik and Ruggieri, Federica and Szekrenyi, Anna and Fessner, Wolf‐Dieter and Berglund, Per
Advanced synthesis & catalysis, ISSN 1615-4150, 02/2020, Volume 362, Issue 4, pp. 812 - 821
Protein engineering | Enzymes | Biocatalysis | Kinetic resolution | Aminotransferase | Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology | Substitutes | Fluorescence | Amines | Chemical synthesis | Substrates
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4. Full Text Stability of Second Generation Grubbs’ Alkylidenes to Primary Amines: Formation of Novel Ruthenium‐Amine Complexes
by Wilson, Gerald O and Porter, Keith A and Weissman, Haim and White, Scott R and Sottos, Nancy R and Moore, Jeffrey S
Advanced synthesis & catalysis, ISSN 1615-4150, 08/2009, Volume 351, Issue 11‐12, pp. 1817 - 1825
ruthenium | self‐healing polymers | ring‐opening metathesis (ROMP) | ring‐closing metathesis (RCM) | primary amines | Grubbs’ catalyst stability | Self-healing polymers | Grubbs' catalyst stability | Primary amines | Ruthenium | Ring-opening metathesis (ROMP) | Ring-closing metathesis (RCM) | Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology
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5. Full Text Direct Aryl C−H Amination with Primary Amines Using Organic Photoredox Catalysis
by Margrey, Kaila A and Levens, Alison and Nicewicz, David A and Univ. of North Carolina, Chapel Hill, NC (United States)
Angewandte Chemie (International ed.), ISSN 1433-7851, 12/2017, Volume 56, Issue 49, pp. 15644 - 15648
organocatalysis | amines | arenes | photochemistry | synthetic methods | Usage | Amines | Catalysis | Drugs | Catalysts | Toluene | Amino acids | Biological activity | Aromatics | Photoredox catalysis | Agrochemicals | Amination | Aromatic compounds | Benzene | Chemical bonds | Coupling | Scaffolds | Aliphatic amines | Index Medicus | Chemistry
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6. Full Text Conversion of alcohols to enantiopure amines through dual-enzyme hydrogen-borrowing cascades
by Francesco G. Mutti and Tanja Knaus and Nigel S. Scrutton and Michael Breuer and Nicholas J. Turner
Science (American Association for the Advancement of Science), ISSN 0036-8075, 9/2015, Volume 349, Issue 6255, pp. 1525 - 1529
REPORTS | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Alcohols - chemistry | Lactobacillus - genetics | Biocatalysis | Oxidoreductases Acting on CH-NH Group Donors - chemistry | Oxidoreductases Acting on CH-NH Group Donors - genetics | Bacillus - genetics | Amines - chemical synthesis | Hydrogen - chemistry | Genetic Engineering | Amination | Bacillus - enzymology | Alcohol Dehydrogenase - genetics | Lactobacillus - enzymology | Alcohol Dehydrogenase - chemistry | Enzymes | Amines | Chemical properties | Enantiomers | Chemical synthesis | Production processes | Methods | Alcohols | Bioengineering | Alcohol | Biophysics | Chemical engineering | Index Medicus | Synthesis (chemistry) | Cascades | Bacillus | Byproducts | Conversion
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7. Full Text Boron‐Catalyzed N‐Alkylation of Amines using Carboxylic Acids
by Fu, Ming‐Chen and Shang, Rui and Cheng, Wan‐Min and Fu, Yao
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2015, Volume 54, Issue 31, pp. 9042 - 9046
amines | alkylation | frustrated Lewis pair | boron | synthetic methods | Amines - chemistry | Boron - chemistry | Carboxylic Acids - chemistry | Molecular Structure | Amines - chemical synthesis | Catalysis | Alkylation | Acids | Chemical industry | Index Medicus | Silanes | Amines | Catalysts | Reducing agents | Selectivity | Carboxylic acids | Compatibility
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8. Full Text Catalyst‐Free Deaminative Functionalizations of Primary Amines by Photoinduced Single‐Electron Transfer
by Wu, Jingjing and Grant, Phillip S and Li, Xiabing and Noble, Adam and Aggarwal, Varinder K
Angewandte Chemie (International ed.), ISSN 1433-7851, 04/2019, Volume 58, Issue 17, pp. 5697 - 5701
radical reactions | Giese reactions | photochemistry | deamination | electron donor–acceptor complexes | Electron transport | Radicals | Amines | Salts | Free radicals | Catalysts | Pyridinium | Electron transfer | Chemical reactions | Absorptivity | Alkylation | Catalysis | Coordination compounds | Allyl compounds | Functional groups | Electrons | Index Medicus | Communications | Communication
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9. Full Text Conversion of Primary Amines to Symmetrical Secondary and Tertiary Amines using a Co‐Rh Heterobimetallic Nanocatalyst
by Chung, Hyunho and Han, Seulgi and Chung, Young Keun and Park, Ji Hoon
Advanced synthesis & catalysis, ISSN 1615-4150, 03/2018, Volume 360, Issue 6, pp. 1267 - 1272
nanocatalyst | Tertiary amines | base ligand-free reaction | heterogeneous | Secondary amines | Amines | Chemical industry | Bimetals | Catalysts | Catalytic activity | Catalysis | Leaching
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10. Full Text Asymmetric Synthesis of 2,3‐Dihydropyrroles by Ring‐Opening/Cyclization of Cyclopropyl Ketones Using Primary Amines
by Xia, Yong and Liu, Xiaohua and Zheng, Haifeng and Lin, Lili and Feng, Xiaoming
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2015, Volume 54, Issue 1, pp. 227 - 230
kinetic resolution | scandium | N,N′‐dioxides | ring opening | cyclization | N,N'-dioxides | Cyclization | Kinetic resolution | Ring opening | Scandium | Amines - chemistry | Scandium - chemistry | Pyrroles - chemical synthesis | Oxides - chemistry | Ketones - chemistry | Pyrroles - chemistry | Catalysis | Cytokinins | Synthesis | Amines | Ketones | Green technology | Organic compounds | Index Medicus | Asymmetry | Reaction kinetics | Nucleophiles
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11. Full Text Production of Primary Amines by Reductive Amination of Biomass‐Derived Aldehydes/Ketones
by Liang, Guanfeng and Wang, Aiqin and Li, Lin and Xu, Gang and Yan, Ning and Zhang, Tao
Angewandte Chemie (International ed.), ISSN 1433-7851, 03/2017, Volume 56, Issue 11, pp. 3050 - 3054
biomass | ethanolamine | heterogeneous catalysis | reductive amination | ruthenium catalyst | Ethanolamines | Nitrogen | Heterogeneous catalysis | Ethanolamine | Transformation | Amines | Ketones | Catalysts | Ruthenium oxide | Biomass | Aldehydes | Carbonyl groups | Ammonia | Lignocellulose | Amination | Catalysis | Zirconium dioxide | Carbonyls
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