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Chemistry : a European journal, ISSN 0947-6539, 10/2015, Volume 21, Issue 42, pp. 14678 - 14693
The formation of CC bonds embodies the core of organic chemistry because of its fundamental application in generation of molecular diversity and complexity. CC bond... 
hypervalent iodine | oxidative coupling | CH activation | metal‐free | CC coupling | C-C coupling | C-H activation | metal-free | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Coupling (molecular) | Organic chemistry | State of the art | Synthesis | Formations | Reaction mechanisms | Bonding | Complexity
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2014, Volume 53, Issue 38, pp. 10209 - 10212
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 06/2014, Volume 20, Issue 26, pp. 7911 - 7915
...‐catalyzed aerobic oxidative NS bond cleavage of sulfonyl hydrazides, followed by cross‐coupling reactions with alkenes and aromatic compounds to form the C sp 2... 
copper | sulfones | CH functionalization | oxygen | thioethers | C-H functionalization | Synthesis (chemistry) | Alkenes | Byproducts | Chemical reactions | Transformations | Hydrazides | Bonding | Sulfones
Journal Article
Chemistry, an Asian journal, ISSN 1861-4728, 04/2015, Volume 10, Issue 4, pp. 824 - 838
.... Most directing is achieved through the σ‐bond coordination of functional groups to the metal catalyst, followed by ortho‐selective CH bond cleavage... 
CH activation | annulation | homogeneous catalysis | directing groups | transition metals | Transition metals | C-H activation | Annulation | Homogeneous catalysis | Directing groups
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 06/2013, Volume 52, Issue 26, pp. 6576 - 6578
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 10/2015, Volume 54, Issue 44, pp. 13049 - 13052
Nitrogenation by direct functionalization of CH bonds represents an important strategy for constructing CN bonds. Rhodium(III... 
CH activation | amides | oximes | synthetic methods | rhodium | C-H activation | Hydrogen Bonding | Amides - chemical synthesis | Amides - chemistry | Organometallic Compounds - chemistry | Molecular Structure | Catalysis | Rhodium - chemistry | Index Medicus | Oximes | Rhodium | Quinoline | Amides | Strategy | Activation | Ethers
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2017, Volume 56, Issue 4, pp. 1073 - 1076
...‐selectively activate the C−H bond located γ to the amino group. Added bulk: A palladium‐catalyzed reaction of primary amines with iodoarenes produces γ... 
amines | reaction mechanisms | palladium | C−H activation | arylation | Palladium | Buttresses | Amines | Hydrogen bonds
Journal Article
Catalysis communications, ISSN 1566-7367, 04/2019, Volume 123, pp. 105 - 108
...–H bond in para-position into C[dbnd]O bond under mild conditions. The catalyst shows high activity for unsubstituted or alkyl substituted phenols, but no effect on substituted phenols with electron-withdrawing groups... 
C-H bond | Phenols | Selective activation | C=O bond | Aerobic oxidation | Nitriles | Oxidation-reduction reaction | Catalysis | Bonds
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 04/2018, Volume 24, Issue 20, pp. 5331 - 5340
.... Similar to most of the previously described low‐spin hydroperoxoiron(III) compounds, 3 behaves as a sluggish oxidant and it is not kinetically competent for breaking weak C−H bonds... 
oxidation | density functional calculations | stereospecific | C−H bond activation | hydroperoxoiron(III) | Hydrogen peroxide | Hydroxylation | Mass spectrometry | Bonds | Heme | Triflic acid | Transformation | Mass spectroscopy | Substrates | Acids | Bonding strength | Chemical bonds | Protonation | Stereospecificity | Oxidation | Species | Low temperature
Journal Article