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Chemical Society reviews, ISSN 0306-0012, 04/2015, Volume 44, Issue 7, pp. 1922 - 1947
Metal organic frameworks (MOFs) are porous crystalline solids whose structure is formed by metal ions or clusters of a few metal ions held in place by bi- or... 
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 12/2017, Volume 23, Issue 69, pp. 17576 - 17583
Journal Article
Accounts of Chemical Research, ISSN 0001-4842, 10/2018, Volume 51, Issue 10, pp. 2589 - 2599
Conspectus Transition-metal-catalyzed cross-coupling reactions represent a most powerful tool for the rapid construction of C–C and C–X bonds available to... 
ROOM-TEMPERATURE | ELECTRONICALLY-ACTIVATED AMIDES | BUCHWALD-HARTWIG | ARYL ESTERS | HETEROCYCLIC CARBENE COMPLEXES | ORGANOMETALLIC CHEMISTRY | PD-NHC PRECATALYST | STERIC PROPERTIES | CHEMISTRY, MULTIDISCIPLINARY | SUZUKI-MIYAURA | GENERAL-METHOD
Journal Article
Tetrahedron, ISSN 0040-4020, 01/2020, Volume 76, Issue 3, p. 130836
Regioselectively polysubstituted pyridines can be efficiently accessed from 2-halopyridines via a sequence involving C–H borylation, Suzuki-Miyaura... 
C–H borylation | Pyridine | Suzuki-Miyaura | Multidirectional synthesis
Journal Article
Chemical Communications, ISSN 1359-7345, 2010, Volume 46, Issue 16, pp. 2742 - 2744
The synthesis and complete characterisation of a well-defined N-heterocyclic carbene bearing gold hydroxide complex, [Au(OH)(IPr)], is reported. Its reaction... 
PALLADIUM COMPLEXES | REACTIVITY | NHC | BEARING | VALUES | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | SUZUKI-MIYAURA | CATALYSTS
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2011, Volume 50, Issue 51, pp. 12184 - 12188
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2014, Volume 53, Issue 16, pp. 4142 - 4145
The shape sensitivity of Pd catalysts in Suzuki–Miyaura coupling reactions is studied using nanocrystals enclosed by well‐defined surface facets. The catalytic... 
Suzuki–Miyaura coupling | surface facet | palladium | heterogeneous catalysis | Suzuki-Miyaura coupling | CARBON | ACID | HECK | NANOCRYSTALS | SIZE | NANOPARTICLE SHAPE | LEACHING MECHANISM | CHEMISTRY, MULTIDISCIPLINARY | PD NANOPARTICLES | SURFACE | WATER | Palladium catalysts | Heterogeneous catalysis | Palladium | Nanocrystals | Index Medicus | Origins | Tracking | Catalysts | Morphology | Joining | Catalysis | Leaching
Journal Article
Tetrahedron, ISSN 0040-4020, 05/2015, Volume 71, Issue 21, pp. 3314 - 3324
We report an innovative, high yielding one-pot sequential catalytic imine arylation/Suzuki–Miyaura cross-coupling reaction, which converts suitably activated... 
Suzuki–Miyaura coupling | Arylation | Palladium | Sequential catalysis | Suzuki-Miyaura coupling | MOLECULAR-ORBITAL METHODS | CHEMISTRY, ORGANIC | ASYMMETRIC ARYLATION | SUZUKI-MIYAURA | ARYLBORONIC ACIDS | DENSITY FUNCTIONALS | TRANSITION-ELEMENTS | ORGANOBORON REAGENTS | TRANSMETALATION | DERIVATIVES | WATER
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 09/2014, Volume 55, Issue 38, pp. 5311 - 5314
An efficient synthetic method for the synthesis of a basic amine dendron grafted on SBA-15 and a related Pd(II) complex as two novel catalysts has been... 
Suzuki–Miyaura coupling | Organosuperbase | SBA-15 | Henry reaction | Suzuki-Miyaura coupling | ACID | SILICA CATALYSTS | CHEMISTRY, ORGANIC | CONDENSATION | STATE | EFFICIENT | Palladium
Journal Article
Catalysis Communications, ISSN 1566-7367, 10/2013, Volume 40, pp. 111 - 115
Pd supported on polyamine modified graphene oxide (GO-NH2-Pd2+) was fabricated for the first time. The prepared catalyst was characterized by transmission... 
Polyamine modified graphene oxide | Suzuki–Miyaura coupling reaction | Pd catalyst | Suzuki-Miyaura coupling reaction | CARBON | ACIDS | CHEMISTRY, PHYSICAL | GRAPHITE OXIDE | IONIC LIQUID | RISE | MODIFIED ZEOLITES | HIGHLY-ACTIVE CATALYSTS | COUPLING REACTION | HECK REACTION | EFFICIENT | Palladium | Graphene | Analysis | Graphite
Journal Article
JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, 04/2019, Volume 84, Issue 8, pp. 4653 - 4660
Unusual Pd deactivation and inhibition pathways were observed in a C-N coupling system. Irreversible catalyst deactivation involved C-H insertion of Pd into... 
CHEMISTRY, ORGANIC | AMINATION | JAK2 INHIBITOR | SUZUKI-MIYAURA | DISCOVERY | BULKY
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2012, Volume 51, Issue 6, pp. 1379 - 1382
Fluoride ions play three roles in the Suzuki–Miyaura reaction. They favor the reaction by formation of trans‐[ArPdF(PPh3)2], which reacts with Ar′B(OH)2 in an... 
palladium | reaction mechanism | fluoride ions | Suzuki–Miyaura reactions | aryl boronic acid | Suzuki-Miyaura reactions | PD(II) | BORONIC ACID | ELIMINATION | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | BASE | CROSS-COUPLING REACTIONS | ARYL CHLORIDES | Formations | Fluorides
Journal Article