A reassessment of the transition-metal free suzuki-type coupling methodology.
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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.Design, synthesis, and biological evaluation of resveratrol analogues as aromatase and quinone reductase 2 inhibitors for chemoprevention of cancer.On the role of metal contaminants in catalyses with FeCl3.Iron-catalyzed alkylations of aryl sulfamates and carbamates.Synthesis of tetrahydroxybiphenyls and tetrahydroxyterphenyls and their evaluation as amyloid-β aggregation inhibitors.Trace metal impurities in catalysis.Synthesis and application of water-soluble NHC transition-metal complexes.To be or not to be metal-free: trends and advances in coupling chemistries.Site-selective Suzuki-Miyaura coupling of heteroaryl halides - understanding the trends for pharmaceutically important classes.Iron-catalyzed heterocycle and arene deprotonative alkylation.Direct transition-metal-free intramolecular arylation of phenols.HandaPhos: A General Ligand Enabling Sustainable ppm Levels of Palladium-Catalyzed Cross-Couplings in Water at Room Temperature.Masuda borylation-Suzuki coupling (MBSC) sequence of vinylhalides and its application in a one-pot synthesis of 3,4-biarylpyrazoles.Heteroleptic nickel(ii)-diNHC complexes and an unusual 'reverse' carbene-transfer reaction to silver(i).“Metal-free” catalytic oxygen reduction reaction on heteroatom- doped graphene is caused by trace metal impurities.Water-stabilized three- and four-atom palladium clusters as highly active catalytic species in ligand-free C-C cross-coupling reactions.Opening an Aladdin's cave: the Suzuki coupling in a room-temperature ionic liquid.Gold-Catalyzed Suzuki Coupling of ortho-Substituted Hindered Aryl Substrates.In situ temperature measurements of reaction spaces under microwave irradiation using photoluminescent probes.Mikrowellen in der Organischen SyntheseMagnetic Nanoparticles-Supported Palladium: A Highly Efficient and Reusable Catalyst for the Suzuki, Sonogashira, and Heck ReactionsCopper-Catalyzed Cross-Coupling Interrupted by an Opportunistic Smiles Rearrangement: An Efficient Domino Approach to DibenzoxazepinonesHydrophilic Pd0Complexes Based on Sugars for Efficient Suzuki-Miyaura Coupling in Aqueous SystemsUse of dimethyl carbonate as a solvent greatly enhances the biaryl coupling of aryl iodides and organoboron reagents without adding any transition metal catalystsEvolution of microwave irradiation and its application in green chemistry and biosciences
P2860
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P2860
A reassessment of the transition-metal free suzuki-type coupling methodology.
description
2005 nî lūn-bûn
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2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
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2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
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2005年學術文章
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2005年學術文章
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name
A reassessment of the transition-metal free suzuki-type coupling methodology.
@en
A reassessment of the transition-metal free suzuki-type coupling methodology.
@nl
type
label
A reassessment of the transition-metal free suzuki-type coupling methodology.
@en
A reassessment of the transition-metal free suzuki-type coupling methodology.
@nl
prefLabel
A reassessment of the transition-metal free suzuki-type coupling methodology.
@en
A reassessment of the transition-metal free suzuki-type coupling methodology.
@nl
P2093
P356
P1476
A reassessment of the transition-metal free suzuki-type coupling methodology.
@en
P2093
Michael S Sangi
Patricia Granados
Riina K Arvela
Robert D Singer
Victoria A Williams
P304
P356
10.1021/JO048531J
P407
P577
2005-01-01T00:00:00Z