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Organic Letters, ISSN 1523-7060, 02/2017, Volume 19, Issue 4, pp. 962 - 965
Selective bromination reactions of “click compounds” are described. Electron-neutral and electron-deficient arenes selectively undergo unprecedented... 
H BOND ACTIVATION | DIRECTING GROUP | PALLADIUM | REGIOSELECTIVE HALOGENATION | 1,2,3-TRIAZOLES | ARENES | CHEMISTRY, ORGANIC | CATALYZED ORTHO-HALOGENATION | COPPER | DIRECT ARYLATIONS
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 03/2018, Volume 83, Issue 6, pp. 3403 - 3408
The synthesis of N-acyl-5-halo-8-aminoquinolines has been realized by directly employing 8-aminoquinolines and acyl halides (Cl, Br, I) with copper catalysis.... 
FUNCTIONALIZATION | POSITION | MILD CONDITIONS | REGIOSELECTIVE HALOGENATION | STRATEGY | CHLORIDES | CHEMISTRY, ORGANIC | QUINOLINE DERIVATIVES | C-H ACTIVATION | SODIUM-HALIDES | AMIDES
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2010, Volume 49, Issue 11, pp. 2028 - 2032
Golden bromination: A highly efficient and mild AuCl3‐catalyzed bromination of aromatic rings with N‐bromosuccinimide (NBS) has been developed. This method... 
gold | aromatic compounds | CH activation | halogenation | synthetic methods | Gold | Synthetic methods | C-H activation | Aromatic compounds | Halogenation | BROMOSUCCINIMIDE NBS | SILICA-GEL | NUCLEAR | BROMINATION REAGENT | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | ACTIVATED AROMATICS | MILD | REGIOSELECTIVE MONOBROMINATION | GOLD(III) | ELECTRON-RICH ARENES
Journal Article
Chemistry (Weinheim an der Bergstrasse, Germany), ISSN 0947-6539, 10/2019, Volume 25, Issue 59, pp. 13591 - 13597
A new generation of N-heterocyclic carbene palladium(II) complexes containing vinyl groups in different positions in the backbone of the N-heterocycle have... 
COMPLEX | HETEROCYCLIC CARBENE-PALLADIUM | flow catalysis | ARENES | supported catalysts | CHEMISTRY, MULTIDISCIPLINARY | directed halogenation | MEDICINAL CHEMISTRY | FUNCTIONALIZATION | NANOPARTICLES | C-H activation | ACETOXYLATION | REGIOSELECTIVE HALOGENATION | BONDS | palladium | SELECTIVITY
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 02/2016, Volume 22, Issue 7, pp. 2282 - 2290
Journal Article
Asian Journal of Organic Chemistry, ISSN 2193-5807, 08/2018, Volume 7, Issue 8, pp. 1524 - 1541
Aryl halides are an indispensably important class of compounds owing to their role as precursors in the synthesis of organometallic reagents and nucleophilic... 
C−H functionalization | transition-metal catalysis | halogenation | site-selectivity | directing groups | ROOM-TEMPERATURE | MANGANESE PORPHYRIN | C(SP)-H BONDS | CHEMISTRY, ORGANIC | REMOVABLE AUXILIARY | C-H functionalization | WEAK COORDINATION | CROSS-COUPLING REACTIONS | ORTHO-BROMINATION | REGIOSELECTIVE HALOGENATION | BOND ACTIVATION
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 01/2017, Volume 82, Issue 2, pp. 1114 - 1126
A palladium-catalyzed, ortho-selective C–H halogenation methodology is reported herein. The highlight of the work is the highly selective C­(sp2)–H... 
FUNCTIONALIZATION | CROSS-COUPLING REACTIONS | ORTHO-BROMINATION | REGIOSELECTIVE HALOGENATION | AQUEOUS-MEDIA | CHEMISTRY, ORGANIC | IODINATION | BOND ACTIVATION | DIRECTING-GROUP | WEAK COORDINATION | AROMATIC NITRILES | Usage | Palladium | Chemical properties | Chemical synthesis | Halogenation
Journal Article
Asian Journal of Organic Chemistry, ISSN 2193-5807, 10/2017, Volume 6, Issue 10, pp. 1361 - 1364
A general and efficient protocol for the synthesis of ortho‐halogenated tertiary benzamides under mild conditions is described. Benzamides with various... 
benzamides | catalysis | palladium | halogenation | ROOM-TEMPERATURE | LITHIUM HALIDES | CHEMISTRY, ORGANIC | REMOVABLE AUXILIARY | ORTHO-CHLORINATION | C-H BONDS | ACTIVATION REACTIONS | CROSS-COUPLING REACTIONS | REGIOSELECTIVE HALOGENATION | KINETIC RESOLUTION | PD(III) COMPLEXES
Journal Article
Green Chemistry, ISSN 1463-9262, 2010, Volume 12, Issue 3, pp. 458 - 462
A simple ammonium deep eutectic solvent was used as a dual catalyst and environmentally benign reaction medium for the bromination of... 
REAGENT | IMIDAZOLIUM IONIC LIQUIDS | CHEMISTRY, MULTIDISCIPLINARY | ACTIVATED AROMATICS | REGIOSELECTIVE MONOBROMINATION
Journal Article
ORGANIC LETTERS, ISSN 1523-7060, 05/2019, Volume 21, Issue 10, pp. 3848 - 3854
An unprecedented deformylative halogenation of aldehydes to alkyl halides is presented. Under oxidative conditions, 1,4-dihydropyridine (DHP), derived from an... 
MEDICINAL CHEMISTRY | CATALYSIS | CROSS-COUPLING REACTIONS | OXIDATIVE CHLORINATION | ACTIVATION | SELECTIVE BROMINATION | VISIBLE-LIGHT PHOTOREDOX | CHEMISTRY, ORGANIC | H BONDS | GENERATION | REGIOSELECTIVE HYDROCHLORINATION
Journal Article
Synthesis, ISSN 0039-7881, 03/2018, Volume 50, Issue 6, pp. 1359 - 1367
Abstract A simple and efficient methodology for the direct halogenation of N -phenylureas was developed using trihaloisocyanuric acids in acetonitrile at room... 
paper | regioselectivity | chemoselectivity | arenes | trihaloisocyanuric acids | halogenation | electrophilic aromatic substitution | ureas | TRICHLOROISOCYANURIC ACID | CHEMISTRY, ORGANIC | IODINATION | UREA DERIVATIVES | REGIOSELECTIVE COIODINATION | NUCLEOPHILES | TRIIODOISOCYANURIC ACID | ISOCYANATES | AGENTS | CONVENIENT REAGENT | ACTIVATED ARENES
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 11/2016, Volume 57, Issue 45, pp. 4965 - 4968
A mild copper(II)-mediated α-halogenation of -aryl enaminones was developed. α-Halogenated -aryl enaminones were obtained in moderate to good yields using CuX... 
Regioselective | α-Halogenated N-aryl enaminones | N-Aryl enaminones | Halogenation | Copper(II) halide | CONSTRUCTION | alpha-Halogenated N-aryl enaminones | CHEMISTRY, ORGANIC | C-H HALOGENATION | SELECTIVE HALOGENATION | BOND | AMIDES
Journal Article
Beilstein Journal of Organic Chemistry, ISSN 1860-5397, 11/2015, Volume 11, Issue 1, pp. 2132 - 2144
Carbon-halogen (C-X) bonds are amongst the most fundamental groups in organic synthesis, they are frequently and widely employed in the synthesis of numerous... 
Copper | H bond | C(sp | Halogenation | PALLADIUM | LITHIUM HALIDES | CHEMISTRY, ORGANIC | IODINATION | halogenation | CROSS-COUPLING REACTIONS | MILD CONDITIONS | OXIDATIVE FUNCTIONALIZATION | PHENOLS | DEHYDROGENATIVE FUNCTIONALIZATION | REGIOSELECTIVE HALOGENATION | copper | C(sp)-H bond | CHLORINATION | C(sp2)–H bond | C(sp3)–H bond
Journal Article
Journal of Organometallic Chemistry, ISSN 0022-328X, 03/2016, Volume 805, pp. 1 - 5
Journal Article
Organic Letters, ISSN 1523-7060, 04/2018, Volume 20, Issue 8, pp. 2468 - 2471
A new method for chlorination of alcohols and carboxylic acids, using α,α-dichlorodiphenylmethane as the chlorinating agent and FeCl3 as the catalyst, was... 
MILD | SALT | TRANSFORMATION | SYSTEM | AROMATIC CATION ACTIVATION | ALLYLIC ALCOHOLS | NUCLEOPHILIC-SUBSTITUTION | CHEMISTRY, ORGANIC | DIRECT REGIOSELECTIVE CHLORINATION | UNPROTECTED HEXITOLS | PENTITOLS
Journal Article
Organic & biomolecular chemistry, ISSN 1477-0520, 02/2016, Volume 14, Issue 7, pp. 2352 - 2359
A mild and efficient protocol for the assembly of tetra-substituted 5-trifluoromethylpyrazoles is presented, involving halogenation at the 4-position of... 
Pyrazoles - chemistry | Nitrogen - chemistry | Halogenation | Ligands | Molecular Structure | Catalysis | Palladium - chemistry | Carbon - chemistry
Journal Article