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2010, ISBN 9783527325092, xxv, 494
This first comprehensive presentation of this hot and important topic compiles the most up-to-date methods for chiral amine synthesis. The international list... 
Chirality | Amines | Synthesis
Book
Angewandte Chemie (International ed.), ISSN 1433-7851, 12/2015, Volume 54, Issue 50, pp. 15046 - 15050
The implementation of inexpensive, Earth‐abundant metals in typical noble‐metal‐mediated chemistry is a major goal in homogeneous catalysis. A sustainable or... 
hydrogen‐transfer catalysis | alcohols | base metals | cobalt | amine alkylation | hydrogen-transfer catalysis | Aromatic amines | Catalysis | Hydrogen | Cobalt | Alcohol
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 12/2013, Volume 52, Issue 52, pp. 14089 - 14093
Various olefins can be smoothly transformed in the presence of a Pd‐based catalyst system and (hetero)aromatic amines or nitroarenes to synthetically... 
amides | nitroarenes | alkenes | aromatic amines | aminocarbonylation | Olefins | Palladium | Aromatic amines | Quinoline | Amides | Amines | Catalysts
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 01/2017, Volume 139, Issue 2, pp. 607 - 610
A pyridine-catalyzed transition-metal-free borylation reaction of haloarenes has been developed based on the selective cross-coupling of an aryl radical and a... 
Usage | Pyridine | Aromatic amines | Chemical properties | Chemical synthesis
Journal Article
Journal of hazardous materials, ISSN 0304-3894, 10/2017, Volume 339, pp. 401 - 408
Journal Article
Food science & technology, ISSN 0023-6438, 11/2014, Volume 59, Issue 1, pp. 229 - 233
Heterocyclic aromatic amines are compounds produced in meat subjected to high temperature cooking. Formation of these substances is highly influenced by... 
Carcinogen | Inhibition | Heterocyclic aromatic amines | Antioxidant | Meat | Life Sciences & Biomedicine | Food Science & Technology | Science & Technology | Antioxidants | Prevention | Aromatic amines | Heterocyclic compounds | Gastrointestinal system | Health aspects | Cancer
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 10/2013, Volume 52, Issue 44, pp. 11581 - 11584
Sandmeyer‐type stannylation: Stille coupling is one of the most powerful coupling reactions for CC bond formation, whereas there are only limited methods to... 
aryl stannanes | diazonium salts | Sandmeyer reaction | cross‐coupling | Stille coupling reaction | cross-coupling | Substitution reactions | Diazo compounds | Aromatic amines | Joining | Transformations | Synthesis | Amines | Aromatic compounds | Bonding
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 10/2015, Volume 357, Issue 14‐15, pp. 3121 - 3125
A palladium/(R)‐Binap catalyst for asymmetric ring opening reaction of azabenzonorbornadienes with amines was developed that afforded the corresponding... 
amines | palladium | silver | azabenzonorbornadienes | asymmetric ring opening reaction | Palladium catalysts | Palladium | Aromatic amines | Synthesis | Amines | Asymmetry | Catalysts | Catalysis | Ring opening
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 02/2000, Volume 122, Issue 7, pp. 1360 - 1370
Bulky, electron-rich phosphine ligands with a biphenyl backbone, when combined with Pd(OAc)2, give highly active catalysts for the α-arylation of ketones. The... 
Usage | Aromatic amines | Research | Catalysts | Ketones
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 11/2014, Volume 53, Issue 45, pp. 12158 - 12162
An unprecedented catalytic system composed of the Wilkinson catalyst [Rh(PPh3)3Cl] and CF3COOH enabled the highly regioselective cross‐coupling of aromatic... 
heteroarylation | organic semiconductors | aromatic amines | oxidative cross‐coupling | Wilkinson catalyst | Oxidative cross-coupling | Organic semiconductors | Aromatic amines | Heteroarylation | Amines - chemistry | Catalysis | Oxidation-Reduction | Semiconductors | Index Medicus
Journal Article
Comptes rendus. Chimie, ISSN 1631-0748, 07/2018, Volume 21, Issue 7, pp. 639 - 643
The aza-Michael addition of functionally substituted anilines to enoates is significantly affected by the hydrogen bond donor ability of the solvent. Very... 
Trifluoroethanol | Aromatic amines | 1,4-Addition | Hexafluoroisopropanol | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology
Journal Article