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European Journal of Organic Chemistry, ISSN 1434-193X, 04/2017, Volume 2017, Issue 15, pp. 2072 - 2084
Journal Article
Chemical Science, ISSN 2041-6520, 2017, Volume 8, Issue 5, pp. 3465 - 3470
An efficient and broadly applicable process is reported for the direct alkylation of C-H bonds in heteroarenes, privileged scaffolds in many areas of science.... 
HALIDES | FUNCTIONALIZATION | C-H BOND | GOLD CATALYSIS | NITROGEN NUCLEOPHILES | SECONDARY | LIGAND | ELECTRON-RICH HETEROCYCLES | RADICAL ALKYLATION | BROMIDES | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Synthesis, ISSN 0039-7881, 08/2017, Volume 49, Issue 15, pp. 3407 - 3421
Abstract Aromatic heterocycles are an important class of compounds found in a wide range of natural products, pharmaceutically active molecules and organic... 
short review | redox-neutral | radical reactions | heteroarenes | C-H functionalization | C-C bonds formation | ROOM-TEMPERATURE | DIRECT ARYLATION | TERTIARY ALKYL-HALIDES | CHEMISTRY, ORGANIC | DIARYLIODONIUM SALTS | N-HETEROARENES | CROSS-COUPLING REACTIONS | ARYL DIAZONIUM SALTS | LIGHT PHOTOREDOX CATALYSIS | ELECTRON-RICH HETEROCYCLES | METAL-FREE
Journal Article
Synthesis, ISSN 0039-7881, 12/2010, Volume 2010, Issue 24, pp. 4131 - 4153
Abstract This review with 272 references covers the literature published up to the end of February 2010 on the methods, other than the Mizoroki-Heck reaction,... 
review | coupling | heteroarenes | catalysis | transition metals | olefination | C-H BOND | PYRIDINE-N-OXIDES | CONCISE TOTAL-SYNTHESIS | CHEMISTRY, ORGANIC | INCLUDING FREE (NH)-IMIDAZOLE | DIRECT C-2 ARYLATION | CROSS-COUPLING REACTIONS | ELECTRON-RICH OLEFINS | STEREOSELECTIVE-SYNTHESIS | ULLMANN-TYPE REACTION | HECK REACTION
Journal Article
CHEMICAL REVIEWS, ISSN 0009-2665, 01/2016, Volume 116, Issue 2, pp. 719 - 766
Diverse radiochemistry is an essential component of nuclear medicine; this includes imaging techniques such as positron emission tomography (PET). As such, PET... 
CROSS-COUPLING REACTIONS | COPPER-MEDIATED FLUORINATION | F BOND FORMATION | F-18 ACETYL HYPOFLUORITE | HIGH-AFFINITY RADIOLIGAND | NICOTINIC ACETYLCHOLINE-RECEPTORS | ELECTRON-RICH ARENES | IN-VIVO EVALUATION | CHEMISTRY, MULTIDISCIPLINARY | HIGH-YIELD SYNTHESIS | NUCLEOPHILIC AROMATIC-SUBSTITUTION
Journal Article
Tetrahedron, ISSN 0040-4020, 02/2016, Volume 72, Issue 5, pp. 613 - 624
Journal Article
Chemical Science, ISSN 2041-6520, 05/2017, Volume 8, Issue 5, pp. 3465 - 3470
An efficient and broadly applicable process is reported for the direct alkylation of C-H bonds in heteroarenes, privileged scaffolds in many areas of science.... 
Thiophenes | Aromatic compounds | Chemical bonds | Furans | Derivatives | Coumarin | Radicals | Alkylation
Journal Article
Tetrahedron, ISSN 0040-4020, 11/2019, Volume 75, Issue 46, p. 130664
An efficient synthesis of N-heterocyclic aryl sulfides via NH4I/1,10-phenanthroline-catalyzed direct sulfenylation reactions was reported. In this reaction,... 
Sulfenylation | Metal-free | Indole | Ethyl arylsulfinates | Pyrrole | GRAPHENE OXIDE | PROMOTED REGIOSELECTIVE SULFENYLATION | C-H SULFENYLATION | CHEMISTRY, ORGANIC | sulfenylation | 2ND SULFENYLATION | S BOND FORMATION | INDOLYL ARYL SULFONES | RECEPTOR LIGANDS | QUINONE MONO-O,S-ACETALS | ELECTRON-RICH ARENES | EFFICIENT SULFENYLATION
Journal Article
Topics in Organometallic Chemistry, ISSN 1436-6002, 2019, Volume 63, pp. 225 - 265
Journal Article
TETRAHEDRON, ISSN 0040-4020, 08/2018, Volume 74, Issue 33, pp. 4373 - 4380
A convenient, practical and highly efficient one-pot method has been developed for the synthesis of triaryl- and triheteroarylmethane derivatives by... 
Triheteroarylmethane | TRIARYLMETHANES | CHEMISTRY, ORGANIC | Trialkyl orthoformate | IODINE | TRIETHYL ORTHOFORMATE | ACID-DERIVATIVES | FACILE SYNTHESIS | Bismuth(III) triflate | GREEN SYNTHESIS | NITRIC-OXIDE | ELECTRON-RICH ARENES | TRIINDOLYLMETHANES | EFFICIENT | Triarylmethane | Friedel-Crafts reaction
Journal Article
Organic Letters, ISSN 1523-7060, 11/2016, Volume 18, Issue 21, pp. 5564 - 5567
The first example of nickel-catalyzed monofluoroalkylation of arylsilanes has been developed with readily available fluoroalkyl halides. This novel... 
MEDIATED FLUOROALKYLATION | ARYL BORONIC ACIDS | ALPHA-ARYLATION | FLUORO-BETA-LACTAM | (2-PYRIDYL)SULFONYL GROUP | CHEMISTRY, ORGANIC | REDOX-ACTIVE ESTERS | PHENYLETHANOLAMINE N-METHYLTRANSFERASE | ELECTRON-RICH HETEROARENES | TRIFLUOROMETHYLTHIOLATION REACTIONS | ALKYL-HALIDES
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 02/2015, Volume 357, Issue 2‐3, pp. 355 - 360
(N‐Trifluoromethylthio)saccharin has been applied as an electrophilic trifluoromethylthiolating reagent for a broad scope of heteroarenes, electron‐donating... 
heteroarenes | electron‐rich olefins | gold catalysts | iron catalysts | trifluoromethylthiolation | Electron-rich olefins | Gold catalysts | Heteroarenes | Trifluoromethylthiolation | Iron catalysts | REAGENT | ROOM-TEMPERATURE | ACTIVATION | SULFIDES | ARENES | CHEMISTRY, ORGANIC | C-H BONDS | BORONIC ACIDS | FUNCTIONALIZATION | ARYL | CHEMISTRY, APPLIED | THIOETHERS | electron-rich olefins | Synthesis | Catalysis | Catalysts | Olefins
Journal Article
Organic Letters, ISSN 1523-7060, 03/2016, Volume 18, Issue 5, pp. 1004 - 1007
A facile synthesis of gem-difluorinated fused quinolines via visible light-mediated cascade radical cyclization between functionalized difluoromethyl chlorides... 
IMIDOYL IODIDES | ETHYL BROMODIFLUOROACETATE | ARYL BORONIC ACIDS | ONE-POT SYNTHESIS | COUPLING REACTIONS | CHEMISTRY, ORGANIC | C-H DIFLUOROALKYLATION | ALKYNES | ELECTRON-RICH HETEROARENES | DERIVATIVES | PHOTOREDOX CATALYSIS
Journal Article
by Xiao, YX and Liu, ZQ
ACTA CHIMICA SINICA, ISSN 0567-7351, 09/2019, Volume 77, Issue 9, pp. 874 - 878
The cross dehydrogenative coupling (CDC) via highly selective C-H bond functionalization represents one of the most atom-economical, environmentally-benign and... 
OXIDATION | ketone and ester | ACTIVATION | ACETONE | BOND FORMATION | electron-rich heteroarene | C-H FUNCTIONALIZATION | CHEMISTRY, MULTIDISCIPLINARY | ALKENES | cross dehydrogenative coupling (CDC) | POLAR | C-H activation | HETEROCYCLES | OLEFINS | free radical
Journal Article