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Chemical Reviews, ISSN 0009-2665, 02/2018, Volume 118, Issue 4, pp. 2249 - 2295
Cross-couplings and related reactions are a class of highly efficient synthetic protocols that are generally promoted by molecular Pd species as catalysts.... 
FREE SONOGASHIRA REACTION | LIGAND-FREE SUZUKI | C-C | SUPPORTED PALLADIUM CATALYSTS | PD/MGLA MIXED-OXIDE | SUZUKI-MIYAURA REACTION | HECK REACTION | IN-SITU GENERATION | CHEMISTRY, MULTIDISCIPLINARY | ARYL CHLORIDES | VISIBLE-LIGHT IRRADIATION | Couplings | Catalysts | Metals | Chemical reactions | Molecular chemistry | Palladium | Industrial applications | Catalysis
Journal Article
Organometallics, ISSN 0276-7333, 10/2015, Volume 34, Issue 23, pp. 5497 - 5508
A brief account of the major developments of palladium-catalyzed cross-coupling during the last two decades is highlighted chronologically, with an emphasis on... 
AIR-STABLE CATALYSTS | ROOM-TEMPERATURE | HIGHLY-ACTIVE CATALYST | ALPHA-ARYLATION | C-N | HETEROCYCLIC CARBENE COMPLEXES | CHEMISTRY, ORGANIC | DEACTIVATED ARYL CHLORIDES | SUZUKI-MIYAURA | LARGE-SCALE APPLICATIONS | GENERAL-METHOD | CHEMISTRY, INORGANIC & NUCLEAR
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 09/2008, Volume 130, Issue 37, pp. 12250 - 12251
Palladium-catalyzed efficient Hiyama cross-coupling reaction of aryl arenesulfonate with arylsilane is described. The desired carbon-carbon bond formation... 
HALIDES | ROOM-TEMPERATURE | SILOXANE | VINYL TOSYLATES | ARYLSILOXANES | MESYLATES | CHLORIDES | BROMIDES | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | SUZUKI-MIYAURA | Arylation | Palladium | Chemical properties | Research | Structure | Silane
Journal Article
ACS Catalysis, ISSN 2155-5435, 06/2018, Volume 8, Issue 6, pp. 5630 - 5635
Three-component cross-coupling cocatalyzed by palladium and norbornene is reported for the synthesis of biaryl atropisomers. This domino reaction gave optimal... 
cross-coupling | palladium | asymmetric catalysis | norbornene | atropisomer | PALLADIUM/NORBORNENE CATALYSIS | ASYMMETRIC-SYNTHESIS | NATURAL-PRODUCTS | EFFICIENT SYNTHESIS | CHEMISTRY, PHYSICAL | SUZUKI-MIYAURA REACTION | C-H FUNCTIONALIZATION | DYNAMIC KINETIC RESOLUTION | AXIALLY CHIRAL BIARYLS | ATROPOSELECTIVE SYNTHESIS | cross-coupling palladium | ARYL IODIDES
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 11/2018, Volume 140, Issue 45, pp. 15126 - 15139
Conjugated polymers are the workhorse materials in organic electronics, a field that is rapidly growing to encompass energy storage devices such as... 
TRANSFER CONDENSATION POLYMERIZATION | TRANSFER POLYCONDENSATION | CHAIN-GROWTH POLYMERIZATION | AB-TYPE MONOMERS | POWER CONVERSION EFFICIENCY | FIELD-EFFECT MOBILITY | DONOR-ACCEPTOR POLYMERS | CONJUGATED MICROPOROUS POLYMERS | HETEROJUNCTION SOLAR-CELLS | CHEMISTRY, MULTIDISCIPLINARY | SUZUKI-MIYAURA
Journal Article
Synthesis, ISSN 0039-7881, 10/2018, Volume 50, Issue 20, pp. 3974 - 3996
Abstract While the advent of transition-metal catalysis has undoubtedly transformed synthetic chemistry, problems persist with the introduction of secondary... 
review | β-H elimination | cross-coupling | mechanism | isomerization | IRON CATALYSIS | CHEMISTRY, ORGANIC | HETEROARYL HALIDES | BORONIC ESTERS | beta-H elimination | NICKEL-PHOSPHINE COMPLEXES | TERTIARY GRIGNARD-REAGENTS | SUZUKI-MIYAURA | CARBON BOND FORMATION | REMOTE FUNCTIONALIZATION | ORGANIC HALIDES | DUAL CATALYSIS
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 04/2017, Volume 139, Issue 15, pp. 5313 - 5316
Journal Article
Angewandte Chemie (International ed. in English), ISSN 1433-7851, 10/2015, Volume 54, Issue 41, pp. 11994 - 11998
Nickel nanoparticles, formed in situ and used in combination with micellar catalysis, catalyze Suzuki Miyaura cross-couplings in water under very mild... 
Green Chemistry | Ni-Nanoparticles | Suzuki-Miyaura couplings | E Factor | Micellar Catalysis
Journal Article
Organic Letters, ISSN 1523-7060, 08/2018, Volume 20, Issue 16, pp. 4719 - 4722
An environmentally responsible, mild method for the synthesis of functionalized 1,3-butadienes is presented. It utilizes allenic esters of varying substitution... 
ORGANIC-CHEMISTRY | DIENES | SUZUKI-MIYAURA COUPLINGS | BIS(PINACOLATO)DIBORON | CONSTRUCTION | AZOBENZENE | LIGHT | CHEMISTRY, ORGANIC | ALPHA | BORYLATION
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 2014, Volume 79, Issue 15, pp. 7132 - 7140
Efficient bis(phosphine)nickel-catalyzed cross-couplings of diarylborinic acids with aryl chlorides, tosylates, and sulfamates have been effected with an... 
ORTHO-SUBSTITUTED BIARYLS | ROOM-TEMPERATURE | PD-PEPPSI-IPENT | CHEMISTRY, ORGANIC | STRUCTURAL-CHARACTERIZATION | STABILIZED NICKEL COMPLEX | RESTRICTED FLEXIBILITY | CATALYTIC-ACTIVITY | SUZUKI-MIYAURA | ARYLBORONIC ACIDS | PHENOL DERIVATIVES
Journal Article
Synlett, ISSN 0936-5214, 09/2016, Volume 27, Issue 15, pp. 2183 - 2200
Abstract Despite the increasing applicability of cross-couplings in organic synthesis, there remain many challenging issues. In the past years, we have... 
account | monophosphorus ligand | asymmetric synthesis | sterical hindrance | michellamine B | Suzuki-Miyaura cross-coupling
Journal Article
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, ISSN 0960-894X, 07/2018, Volume 28, Issue 13, pp. 2320 - 2323
In this study, affinities and activities of derivatized analogues of Dmt-dermorphin[1-4] (i.e. Dmt-D-Ala-Phe-GIyNH(2), Dmt = 2',6'-dimethyl-(S)-tyrosine) for... 
Suzuki-Miyaura cross coupling | CHEMISTRY, MEDICINAL | ANTAGONIST | SOLID-PHASE SYNTHESIS | MORPHINE | PHYSICAL-DEPENDENCE | CHEMISTRY, ORGANIC | Non-natural amino acids | SIDE-CHAINS | GPCR ligands | LIGANDS | AMINO-ACIDS | DERMORPHIN | Opioid peptides | Receptor selectivity | SCAFFOLDS | RECEPTORS
Journal Article
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 07/2018, Volume 28, Issue 13, pp. 2320 - 2323
In this study, affinities and activities of derivatized analogues of Dmt-dermorphin[1–4] (i.e. Dmt- -Ala-Phe-GlyNH , Dmt = 2′,6′-dimethyl-( )-tyrosine) for the... 
Suzuki-Miyaura cross coupling | Opioid peptides | Receptor selectivity | GPCR ligands | Non-natural amino acids | Index Medicus | Receptor Selectivity
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2016, Volume 55, Issue 16, pp. 4914 - 4918
The new monophosphine ligand HandaPhos has been identified such that when complexed in a 1:1 ratio with Pd(OAc) 2 , enables Pd‐catalyzed cross‐couplings to be... 
Suzuki–Miyaura coupling | ligand design | micellar catalysis | E Factor | green chemistry | Suzuki-Miyaura coupling | SUZUKI | DESIGN | HECK | SCOPE | CHEMISTRY, MULTIDISCIPLINARY | Ligands | Limit of Detection | Temperature | Catalysis | Palladium - analysis | Water - chemistry | Palladium | Green technology | Index Medicus | Green Chemistry | Suzuki-Miyaura couplings | Ligand | Micellar Catalysis
Journal Article
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