A New Highly Efficient Catalyst System for the Coupling of Nonactivated and Deactivated Aryl Chlorides with Arylboronic Acids Palladium-Catalyzed Reactions for Fine Chemical Synthesis, Part 17. The authors thank C. Fuhrmann for the excellent support
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Exhibition of the Brønsted acid-base character of a Schiff base in palladium(II) complex formation: lithium complexation, fluxional properties and catalysis of Suzuki reactions in water.Combinatorial libraries with P-functionalized aminopyridines: ligands for the preparation of efficient C(aryl)-Cl activation catalysts.Organotrifluoroborates and monocoordinated palladium complexes as catalysts--a perfect combination for Suzuki-Miyaura coupling.Air-stable, recyclable, and time-efficient diphenylphosphinite cellulose-supported palladium nanoparticles as a catalyst for Suzuki-Miyaura reactions.2-Aryl-indenylphosphine ligands: design, synthesis and application in Pd-catalyzed Suzuki-Miyaura coupling reactions.Chlorination increases the persistence of semiquinone free radicals derived from polychlorinated biphenyl hydroquinones and quinones.Dichloro-bis(aminophosphine) complexes of palladium: highly convenient, reliable and extremely active suzuki-miyaura catalysts with excellent functional group tolerance.Hydrogen-borrowing and interrupted-hydrogen-borrowing reactions of ketones and methanol catalyzed by iridium.Fascinating frontiers of N/O-functionalized N-heterocyclic carbene chemistry: from chemical catalysis to biomedical applications.Keggin type mono Ni(II)-substituted phosphomolybdate: a sustainable, homogeneous and reusable catalyst for Suzuki-Miyaura cross-coupling.Solvent effect on palladium-catalyzed cross-coupling reactions and implications on the active catalytic species.Suzuki cross-coupling mediated by tetradentate N-heterocyclic carbene (NHC)-palladium complexes in an environmentally benign solvent.Palladium--phosphinous acid-catalyzed Sonogashira cross-coupling reactions in water.A simple and highly efficient P,O-type ligand for Suzuki-Miyaura cross-coupling of aryl halides.A one-pot coupling-addition-cyclocondensation sequence (CACS) to 2-substituted 3-acylpyrroles initiated by a copper-free alkynylation.Masuda borylation-Suzuki coupling (MBSC) sequence of vinylhalides and its application in a one-pot synthesis of 3,4-biarylpyrazoles.When are tricoordinated PdII species accessible? Stability trends and mechanistic consequences.Promotion of selective pathways in isomerizing functionalization of plant oils by rigid framework substituents.Pd-Catalyzed Cyanation of (Hetero)Aryl Halides by Using Biphosphine Ligands.Catalyst Controlled Regiodivergent Arylboration of Dienes.An immobilized symmetrical bis-(NHC) palladium complex as a highly efficient and recyclable Suzuki-Miyaura catalyst in aerobic aqueous media.Markovnikov-Selective Palladium Catalyst for Carbonylation of Alkynes with Heteroarenes.Efficient cross-coupling of aryl/alkenyl triflates with acyclic secondary alkylboronic acids.Pd-Co3[Co(CN)6]2 hybrid nanoparticles: preparation, characterization, and challenge for the Suzuki-Miyaura coupling of aryl chlorides under mild conditions.Palladium-Catalyzed Amidation by Chemoselective C(sp3)H Activation: Concise Route to Oxindoles Using a Carbamoyl Chloride PrecursorPalladium-Catalyzed Amidation by Chemoselective C(sp3)H Activation: Concise Route to Oxindoles Using a Carbamoyl Chloride Precursor
P2860
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P2860
A New Highly Efficient Catalyst System for the Coupling of Nonactivated and Deactivated Aryl Chlorides with Arylboronic Acids Palladium-Catalyzed Reactions for Fine Chemical Synthesis, Part 17. The authors thank C. Fuhrmann for the excellent support
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2000 nî lūn-bûn
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2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
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2000年の論文
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A New Highly Efficient Catalys ...... mann for the excellent support
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A New Highly Efficient Catalys ...... mann for the excellent support
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A New Highly Efficient Catalys ...... mann for the excellent support
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A New Highly Efficient Catalys ...... mann for the excellent support
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A New Highly Efficient Catalys ...... mann for the excellent support
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A New Highly Efficient Catalys ...... mann for the excellent support
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A New Highly Efficient Catalys ...... mann for the excellent support
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A New Highly Efficient Catalys ...... mann for the excellent support
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A New Highly Efficient Catalys ...... mann for the excellent support
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A New Highly Efficient Catalys ...... mann for the excellent support
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P2860
P304
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10.1002/1521-3773(20001117)39:22<4153::AID-ANIE4153>3.0.CO;2-T
P577
2000-11-01T00:00:00Z