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Chemistry : a European journal, ISSN 0947-6539, 01/2014, Volume 20, Issue 2, pp. 416 - 420
... catalyzed CH bond functionalization, 3 a direct thiolation of arene CH bonds would provide an alternative method for the rapid preparation of aryl thioethers... 
CH activation | CS bond formation | arenes | rhodium | thiolation | Arenes | C-H activation | Rhodium | Thiolation | C-S bond formation | Strategy | Tolerances | Compatibility | Aromatic compounds | Functional groups | Disulfides
Journal Article
Polymers for advanced technologies, ISSN 1042-7147, 01/2018, Volume 29, Issue 1, pp. 463 - 469
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 02/2014, Volume 20, Issue 9, pp. 2459 - 2462
...H bonds with disulfides or thiols is achieved under palladium catalysis (see scheme). The reaction allows the straightforward and chemoselective introduction of a thiolate group into arenes possessing directing groups. Mechanistic studies reveal that this reaction proceeds through a PdII/PdIV mechanism. 
disulfides | palladium | direct thiolation | aryl sulfides | 2‐arylpyridine | 2-arylpyridine | Thiols | Equivalence | Aromatic compounds | Disulfides | Palladium | Catalysis | Copper | Bearing
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2017, Volume 56, Issue 3, pp. 832 - 836
A photocatalytic method for the aerobic oxidative cleavage of C=C bonds has been developed... 
disulfide catalysts | organocatalysis | olefin oxidation | donor–acceptor complexes | visible-light photocatalysis | Analysis | Catalysis
Journal Article
Macromolecular chemistry and physics, ISSN 1022-1352, 05/2016, Volume 217, Issue 10, pp. 1191 - 1196
.... Disulfide bonds, which become dynamic upon exposure to heat, UV light, or redox conditions, can be used to introduce healable properties to polymer network... 
shape memory | disulfide exchange | polyurethanes | self‐healing | self-healing | Polymer Science | Physical Sciences | Science & Technology | Polyurethanes | Polyurethane resins | Cracks | Heating | Shape memory effect | Disulfides | Chemical bonds | Healing | Recovery
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 03/2015, Volume 51, Issue 19, pp. 4069 - 4072
A nickel-catalyzed thiolation of unactivated C(sp(2))-H bonds with disulfides employing the PIP directing group was described... 
Sulfides | Pathways | Catalysts | Aromatic compounds | Disulfides | Chemical bonds | Nickel | Functional groups
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 12/2018, Volume 57, Issue 50, pp. 16426 - 16430
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2015, Volume 54, Issue 5, pp. 1516 - 1520
...‐electron oxidation and reduction. Homolytic bond activation of diphenyldisulfide by the single... 
mixed valency | bond activation | palladium | phosphane ligands | redox‐active ligands | Mixed valency | Palladium | Redox-active ligands | Bond activation | Phosphane ligands | Catalysis | Ligands | Index Medicus | Reduction | Strategy | Activation | Bonding | Phosphines | Radicals
Journal Article
Chemical communications (Cambridge, England), ISSN 1364-548X, 2015, Volume 51, Issue 34, pp. 7341 - 7344
The first nickel-catalyzed thiolation of unactivated C(sp 3 )–H bonds with disulfides is described... 
Pathways | Catalysts | Disulfides | Chemical bonds | Ligands | Transformations | Nickel | Aliphatic compounds
Journal Article