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1. Full Text Synthesis of meta‐Terphenyl‐2,2′′‐diols by Anodic C−C Cross‐Coupling Reactions
by Lips, Sebastian and Wiebe, Anton and Elsler, Bernd and Schollmeyer, Dieter and Dyballa, Katrin M and Franke, Robert and Waldvogel, Siegfried R
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2016, Volume 55, Issue 36, pp. 10872 - 10876
The anodic C−C cross‐coupling reaction is a versatile synthetic approach to symmetric and non‐symmetric biphenols and arylated phenols. We herein present a... 
meta-terphenyl compounds | protecting groups | pincer ligands | C−C coupling | electrochemistry | C-C coupling | ALKYLIDENE | PINCER-TYPE LIGAND | 2,4-DIMETHYLPHENOL | COMPLEXES | COORDINATION | PHENOL-ARENE | CHEMISTRY, MULTIDISCIPLINARY | SIGMA-BOND METATHESIS | TRIANIONIC PINCER | 1,1,1,3,3,3-HEXAFLUOROPROPAN-2-OL | INTERMEDIATE | Carbon-carbon composites | Coupling (molecular) | Cross coupling | Electrolysis | Phenols | Electrochemistry | Chemical reactions | Selectivity | Chemical synthesis | Functional groups | Diols
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2. Full Text Coupling of Nitrogen Heteroaromatics and Alkanes without Transition Metals: A New Oxidative Cross‐Coupling at CH/CH Bonds
by Deng, Guojun and Ueda, Kirika and Yanagisawa, Shuichi and Itami, Kenichiro and Li, Chao‐Jun
Chemistry – A European Journal, ISSN 0947-6539, 01/2009, Volume 15, Issue 2, pp. 333 - 337
Look—no transition metal! Transition‐metal‐free systems for the direct cross‐coupling reactions of nitrogen heteroaromatics and alkanes are described. Under... 
CH activation | alkanes | nitrogen heterocycles | CC coupling | C-C coupling | Alkanes | C-H activation | Nitrogen heterocycles | ORGANIC-SYNTHESIS | DIRECT ARYLATION | PYRIDINE-N-OXIDES | TERTIARY-AMINES | UNACTIVATED ARENES | AROMATIC-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | HIGHLY EFFICIENT | PALLADIUM-CATALYZED ALKYLATION | RADICAL REACTIONS | ACTIVATED METHYLENE
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3. Full Text Gold‐Catalyzed C(sp3)H/C(sp)H Coupling/Cyclization/Oxidative Alkynylation Sequence: A Powerful Strategy for the Synthesis of 3‐Alkynyl Polysubstituted Furans
by Ma, Yuanhong and Zhang, Shuai and Yang, Shiping and Song, Feijie and You, Jingsong
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2014, Volume 53, Issue 30, pp. 7870 - 7874
In sharp contrast to the gold‐catalyzed reactions of alkynes/allenes with nucleophiles, gold‐catalyzed oxidative cross‐couplings and especially CH/CH... 
gold | oxygen heterocycles | homogeneous catalysis | cross‐coupling | synthetic methods | cross-coupling | DOMINO PROCESS | ALKYNES | POT CYCLIZATION REACTION | CHEMISTRY, MULTIDISCIPLINARY | H BOND ACTIVATION | FUNCTIONALIZATION | HETEROCYCLES | COUPLING REACTIONS | C-C | NONACTIVATED ARENES | DERIVATIVES | Gold | Synthesis | Strategy | Joining | Furans | Terminals | Nucleophiles | Alkynes | Organic compounds
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4. Full Text Highly active palladium catalysts supported by bulky proazaphosphatrane ligands for stille cross-coupling: Coupling of aryl and vinyl chlorides, room temperature coupling of aryl bromides, coupling of aryl triflates, and synthesis of sterically hindered biaryls
by Su, Weiping and Urgaonkar, Sameer and McLaughlin, Patrick A and Verkade, John G
Journal of the American Chemical Society, ISSN 0002-7863, 12/2004, Volume 126, Issue 50, pp. 16433 - 16439
A family of proazaphosphatrane ligands [P(RNCH2CH2)(2)N(R'NCH2CH2): R = wR' = i-Bu, 1; R = Bz, R' = i-Bu, 3; R = R' = Bz, 4] for palladium-catalyzed Stille... 
EFFICIENT CATALYST | MILD CONDITIONS | C-N | BOND FORMATION | ORGANOTIN REAGENTS | HECK REACTION | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | ORGANIC ELECTROPHILES | DIRECT ALPHA-ARYLATION | GENERAL-METHOD | Ligands | Palladium | Research | Chemical properties | Catalysts
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5. Full Text Arsenic‐Mediated C−C Coupling of Cyanides Leading to Cyanido Arsazolide [AsC4N4]
by Arlt, Sören and Harloff, Jörg and Schulz, Axel and Stoffers, Alrik and Villinger, Alexander
Chemistry – A European Journal, ISSN 0947-6539, 09/2017, Volume 23, Issue 52, pp. 12735 - 12738
The chemistry of arsenic cyanides has been investigated and is found to be completely different to the chemistry of the heavier analogs antimony and bismuth as... 
C−C coupling | arsenic | isomerization | heterocycles | cyanides | C-C coupling | MOLECULAR-STRUCTURE | TRIPLE BOND | CRYSTAL | ADDUCTS | CHEMISTRY, MULTIDISCIPLINARY | TRICYANIDE | CATIONS | NITROGEN | Arsenic | Isomerization | Cyanides | Carbon-carbon composites | Cyanide | Salts | Bismuth | Ionic liquids | Chemical bonds | Phosphorus | Antimony | Coupling | Low temperature
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6. Full Text Palladium Complexes of N‐Heterocyclic Carbenes as Catalysts for Cross‐Coupling Reactions—A Synthetic Chemist's Perspective
by Kantchev, Eric Assen B and O'Brien, Christopher J and Organ, Michael G
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2007, Volume 46, Issue 16, pp. 2768 - 2813
Palladium‐catalyzed CC and CN bond‐forming reactions are among the most versatile and powerful synthetic methods. For the last 15 years, N‐heterocyclic... 
palladium | CN coupling | homogeneous catalysis | N‐heterocyclic carbenes | CC coupling | C-C coupling | Palladium | C-N coupling | Homogeneous catalysis | N-heterocyclic carbenes | UNACTIVATED ALKYL BROMIDES | SUZUKI-MIYAURA COUPLINGS | TRANSITION-METAL-COMPLEXES | ARYL DIAZONIUM IONS | HIGH TURNOVER NUMBER | STABLE NUCLEOPHILIC CARBENE | CHEMISTRY, MULTIDISCIPLINARY | PALLADIUM/IMIDAZOLIUM SALT SYSTEM | AMPHIPHILIC POLYMER SUPPORTS | HECK REACTION | PD-II COMPLEXES | Models, Molecular | Ligands | Catalysis | Heterocyclic Compounds - chemistry | Palladium - chemistry
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7. Full Text Photoredox/Nickel Dual Catalysis for the C(sp3)–C(sp3) Cross‐Coupling of Alkylsilicates with Alkyl Halides
by Lévêque, Christophe and Corcé, Vincent and Chenneberg, Ludwig and Ollivier, Cyril and Fensterbank, Louis
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2017, Volume 2017, Issue 15, pp. 2118 - 2121
Alkylsilicates were engaged under photoredox/nickel dual catalysis conditions with alkyl halides for the first time. The C(sp3)–C(sp3) cross‐coupling products... 
Photoredox catalysis | C–C coupling | Nickel | Radical reactions | Cross‐coupling | Cross-coupling | C-C coupling | OXIDATION | ACTIVATION | REAGENTS | CARBON | NICKEL CATALYSIS | CHEMISTRY, ORGANIC | SINGLE-ELECTRON TRANSMETALATION | ARYL BROMIDES | SILICATES | ESTERS | VISIBLE-LIGHT-PHOTOREDOX | Organic chemistry | Chemical Sciences | Catalysis
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8. Full Text [3]Dendralene Synthesis: Rhodium(III)‐Catalyzed Alkenyl CH Activation and Coupling Reaction with Allenyl Carbinol Carbonate
by Wang, Honggen and Beiring, Bernhard and Yu, Da‐Gang and Collins, Karl D and Glorius, Frank
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2013, Volume 52, Issue 47, pp. 12430 - 12434
[3]DendrAl(l)ene! A new synthesis of [3]dendralenes is based on a RhIII‐catalyzed alkenyl CH activation and coupling reaction with allenyl carbinol carbonates... 
trienes | CH activation | dendralenes | dienes | CC coupling | C-C coupling | C-H activation | PRACTICAL SYNTHESIS | DIAZO-COMPOUNDS | HYDROGEN BONDS | CHEMISTRY, MULTIDISCIPLINARY | CC coupling | CH activation | CROSS-CONJUGATED TRIENES | ROBUSTNESS SCREEN | DIELS-ALDER REACTION | RAPID ASSESSMENT | N BOND FORMATION | STEREOSELECTIVE-SYNTHESIS | RHODIUM CATALYSIS | Synthesis | Accessibility | Activation | Joining | Carbonates | Compatibility | Functional groups
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9. Full Text Recent Progress in Nickel‐Catalyzed Biaryl Coupling
by Yamaguchi, Junichiro and Muto, Kei and Itami, Kenichiro
European Journal of Organic Chemistry, ISSN 1434-193X, 01/2013, Volume 2013, Issue 1, pp. 19 - 30
Nickel catalysis for biaryl coupling reactions has received significant attention as a less expensive and less toxic alternative to “standard” palladium... 
C–C coupling | Arylation | Nickel | Biaryls | Homogeneous catalysis | C–H functionali­zation | C-C coupling | C-H functionalization | ARYL GRIGNARD-REAGENTS | POLYCYCLIC AROMATIC-HYDROCARBONS | DECARBOXYLATIVE ARYLATION | CHEMISTRY, ORGANIC | CARBON-CARBON BONDS | ARYLBORONIC ACIDS | SUZUKI-MIYAURA | ORGANOZINC REAGENTS | C-H ARYLATION | 2-ARYLPYRIDINE DERIVATIVES | CYANOBACTERIUM NOSTOC-MUSCORUM | Catalysis
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