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Angewandte Chemie International Edition, ISSN 1433-7851, 04/2014, Volume 53, Issue 16, pp. 4191 - 4195
The alkenylation reactions of 8‐methylquinolines with alkynes, catalyzed by [{Cp*RhCl2}2], proceeds efficiently to give 8‐allylquinolines in good yields by... 
regioselectivity | CH activation | synthetic methods | alkynes | rhodium | C-H activation | ACETYLENES | CATALYZED ADDITION | INSERTION | ARYLATION | CIS-ADDITION | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | MILD CONDITIONS | OXIDATIVE FUNCTIONALIZATION | ARYL KETONES | DERIVATIVES | Activation | Catalysis | Catalysts | Bonding | Alkynes
Journal Article
Solid State Ionics, ISSN 0167-2738, 10/2015, Volume 278, pp. 98 - 105
Interfacial reactions of solid electrolytes play an important role in all-solid-state batteries. The interface resistances—describing charge transfer between... 
All-solid-state battery | Buried interfaces | In situ XPS | Interphase formation | Lithium metal anode | Interfacial reactions | PHYSICS, CONDENSED MATTER | INSERTION | MECHANISM | CHEMISTRY, PHYSICAL | IONIC-CONDUCTIVITY | BATTERIES | METALS | OXIDES | ANODE | Electrolytes | Spectrum analysis | Batteries | Interphase | Electronics | Lithium | Formations | Solid electrolytes | Interface reactions | Electric batteries | Deposition
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 10/2013, Volume 78, Issue 20, pp. 10024 - 10030
Cross-coupling reactions involving metal–carbene are emerging as a new type of carbon–carbon bond-forming reaction. The aim of this JOCSynopsis is to provide... 
PALLADIUM-CATALYZED INSERTION | ACTIVATION | ETHERS | REAGENTS | ALKYLATION | CHEMISTRY, ORGANIC | DIAZO-COMPOUNDS | ARYL IODIDES | VINYL HALIDES | N-TOSYLHYDRAZONES
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 06/2013, Volume 42, Issue 12, pp. 4918 - 4931
Catalysed X-H insertion reactions into diazo compounds (where X is any heteroatom) are a powerful yet underutilized class of transformations. The following... 
ACTIVATION | RHODIUM | IRON PORPHYRIN | BONDS | PEPSIN | DIAZO-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | ENANTIOSELECTIVE INSERTION | Catalysts | Insertion | Historic | Transformations | Biology | Catalysis | Assessments | Strength
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2015, Volume 54, Issue 36, pp. 10623 - 10626
Palladium‐catalyzed direct dialkenylation of cage B(4,5)H bonds in o‐carboranes has been achieved with the help of a carboxylic acid directing group, leading... 
alkenylation | palladium catalysis | cross‐coupling | BH activation | carboranes | cross-coupling | B-H activation | Alkenes - chemistry | Catalysis | Palladium - chemistry | Boranes - chemistry | Cage | Olefins | Decarboxylation | Insertion | Chemical reactions | Activation | Carboxylic acids
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2017, Volume 56, Issue 1, pp. 46 - 48
Versatile C−H insertions: Novel protocols for metal‐carbene insertions using diazo compounds have been recently developed. Application of the respective... 
C−H functionalization | carbenes | palladium | diazo compounds | rhodium | ALPHA-DIAZOCARBONYL COMPOUNDS | ORGANIC-SYNTHESIS | CATALYZED REACTIONS | CYCLOPROPANATION | DIAZO-COMPOUNDS | C-H functionalization | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | MIGRATORY INSERTION | Diazo compounds | Chemical bonds | Palladium | Catalysis | Rhodium | Metals
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 09/2017, Volume 23, Issue 50, pp. 12259 - 12263
Various tetrayne systems were converted under dual gold‐catalyzed conditions. For symmetric tetraalkynyl‐substituted thiophenes, bearing two alkyl‐substituted... 
gold | C−H insertion | cycloisomerization | spiro compounds | alkynes | Thiophene | Catalysis | Carbon-carbon composites | Cores | Gold | Hydrogen bonds | Thiophenes | Chemical reactions | Cyclopentane | Cascade chemical reactions | Spiro compounds | Alkynes | Dibenzothiophene
Journal Article
Accounts of Chemical Research, ISSN 0001-4842, 08/2012, Volume 45, Issue 8, pp. 1365 - 1377
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2008, Volume 47, Issue 5, pp. 932 - 934
Taking on water: A novel catalytic asymmetric metal–carbenoid insertion reaction with water has been developed with copper complexes of chiral spiro... 
carbenoids | hydroxyesters | insertion | asymmetric catalysis | water | Water | Insertion | Carbenoids | Hydroxyesters | Asymmetric catalysis | SI-H | ESTERS | BONDS | CHEMISTRY, MULTIDISCIPLINARY | DIAZOCARBONYL | Copper - chemistry | Esters - chemistry | Stereoisomerism | Water - chemistry | Molecular Structure | Catalysis | Esters - chemical synthesis | Spiro Compounds - chemistry
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2018, Volume 57, Issue 41, pp. 13603 - 13607
A new protocol for the synthesis of a variety of N‐containing aromatic heterocycles by a formal gold‐catalyzed dehydro‐Diels–Alder reaction of ynamide... 
gold | reaction mechanisms | cycloaddition | reaction kinetics | heterocycles | ACTIVATION | CARBAZOLES | VINYLIDENE COMPLEXES | CHEMISTRY, MULTIDISCIPLINARY | ACETYLIDES | GENERATION | CYCLIZATION | ACCESS | C-H INSERTION | DIYNES | Chemical reaction, Rate of | Diels-Alder reaction | Catalysis | Deuterium | Gold | Chemical reactions | Derivatives | Alkynes | Organic chemistry | Chemical Sciences
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 03/2005, Volume 127, Issue 8, pp. 2709 - 2716
Journal Article