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European Journal of Organic Chemistry, ISSN 1434-193X, 04/2017, Volume 2017, Issue 16, pp. 2280 - 2289
A copper‐promoted thiolation of C(sp 2 )–H bonds with disulfides was achieved by using 2‐amino alkylbenzimidazole (MBIP amine) as a new and removable N , N... 
C‐H activation | Nitrogen heterocycles | Copper | Sulfur | Directing groups | C-H activation | ACTIVATION | FUNCTIONALIZATIONS | COMPLEXES | CHEMISTRY, ORGANIC | C-H BONDS | DISULFIDES | THIOLS | ARYL | INHIBITORS | CATALYZED SULFENYLATION | THIOETHERS
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 02/2017, Volume 82, Issue 4, pp. 2263 - 2268
The sulfuration reaction of 2-(2-iodobenzoyl) substituted, or 2-(2-iodobenzyl) substituted 1,2,3,4-tetrahydroisoquinolines with potassium sulfide proceeded in... 
ELEMENTAL SULFUR | ACID-DERIVATIVES | 3-COMPONENT SYNTHESIS | C-H BOND | BETA-PHENYLETHYLAMINES | CHEMISTRY | CHEMISTRY, ORGANIC | BENZOTHIAZINE DERIVATIVES | CARBON-DISULFIDE | DIRECT IMINE ACYLATION | CARBOXYLIC-ACIDS
Journal Article
Chemical Communications, ISSN 1359-7345, 04/2015, Volume 51, Issue 34, pp. 7341 - 7344
The first nickel-catalyzed thiolation of unactivated C(sp(3))-H bonds with disulfides was described. This transformation uses (dppp) NiCl2 as a catalyst and... 
BIDENTATE-CHELATION ASSISTANCE | ALIPHATIC AMIDES | DIRECT ARYLATION | COUPLING REACTIONS | AROMATIC AMIDES | ARYL HALIDES | CARBON-HYDROGEN BONDS | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | DIARYL DISULFIDES | ALKYL-HALIDES | Pathways | Catalysts | Disulfides | Chemical bonds | Ligands | Transformations | Nickel | Aliphatic compounds
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 01/2014, Volume 20, Issue 2, pp. 416 - 420
The rhodium‐catalyzed intermolecular direct CH thiolation of arenes with aryl and alkyl disulfides was developed for the first time to provide a convenient... 
CH activation | CS bond formation | arenes | rhodium | thiolation | Arenes | C-H activation | Rhodium | Thiolation | C-S bond formation | ROOM-TEMPERATURE | ACTIVATION | AMIDATION | ALDEHYDES | INTERNAL ALKYNES | N-CHLOROAMINES | CHEMISTRY, MULTIDISCIPLINARY | FUNCTIONALIZATION | AMINATION | ARYL | O-METHYL OXIMES | Strategy | Tolerances | Compatibility | Aromatic compounds | Functional groups | Disulfides
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 11/2012, Volume 134, Issue 44, pp. 18237 - 18240
An auxiliary-assisted, copper catalyzed or promoted sulfenylation of benzoic acid derivative β-C-H bonds and benzylamine derivative γ-C-H bonds has been... 
Benzoic Acid - chemistry | Benzylamines - chemistry | Copper - chemistry | Catalysis | Disulfides - chemistry | Halogenation | Index Medicus
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 12/2017, Volume 2017, Issue 45, pp. 6576 - 6592
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 08/2014, Volume 356, Issue 11‐12, pp. 2719 - 2724
Journal Article
Biochemistry, ISSN 0006-2960, 06/2006, Volume 45, Issue 24, pp. 7429 - 7433
Journal Article
NATURE, ISSN 0028-0836, 01/2011, Volume 469, Issue 7330, pp. 419 - 419
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 02/2014, Volume 20, Issue 9, pp. 2459 - 2462
A catalytic variant of the direct thiolation of arenes, bearing directing groups, with disulfides or thiols has been developed under palladium and copper... 
disulfides | palladium | direct thiolation | aryl sulfides | 2‐arylpyridine | 2-arylpyridine | Thiols | Equivalence | Aromatic compounds | Disulfides | Palladium | Catalysis | Copper | Bearing
Journal Article
Organic Letters, ISSN 1523-7060, 06/2018, Volume 20, Issue 11, pp. 3362 - 3366
An efficient and chemodivergent palladium-catalyzed thiolation (C-S) and imidation (C-N) of directing group assisted C-H bonds have been accomplished employing... 
ROOM-TEMPERATURE | ACTIVATION | CATALYZED AMIDATION | TRIMETHOXYBENZENE | ARENES | CHLOROAMINES | ARYL SULFIDES | CHEMISTRY, ORGANIC | CARBAZOLES | C-H AMINATION | DISULFIDES
Journal Article
Journal Article
Polymers for Advanced Technologies, ISSN 1042-7147, 01/2018, Volume 29, Issue 1, pp. 463 - 469
Journal Article