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Miyaura

A few examples of reactivity transfer through more than three carbon atoms are also known (a -synthon N. Miyaura, 1975, 1976). [Pg.16]


See other pages where Miyaura is mentioned: [Pg.375]    [Pg.120]    [Pg.218]    [Pg.272]    [Pg.273]    [Pg.277]    [Pg.277]    [Pg.277]    [Pg.277]    [Pg.280]    [Pg.281]    [Pg.281]    [Pg.281]    [Pg.281]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.282]    [Pg.415]    [Pg.415]    [Pg.415]    [Pg.448]    [Pg.449]    [Pg.471]    [Pg.507]    [Pg.509]    [Pg.329]    [Pg.329]    [Pg.329]    [Pg.329]    [Pg.329]    [Pg.332]    [Pg.188]    [Pg.37]    [Pg.723]    [Pg.1205]    [Pg.162]    [Pg.12]    [Pg.14]    [Pg.29]    [Pg.30]   
See also in sourсe #XX -- [ Pg.52 ]

See also in sourсe #XX -- [ Pg.52 ]

See also in sourсe #XX -- [ Pg.296 , Pg.448 ]

See also in sourсe #XX -- [ Pg.368 ]

See also in sourсe #XX -- [ Pg.368 ]




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An Asymmetric Suzuki-Miyaura Reaction

An Asymmetric Suzuki-Miyaura Reaction Mechanism

Application of the Suzuki-Miyaura Reaction

Aqueous conditions Suzuki-Miyaura reaction

Aryl boronic acid, Suzuki-Miyaura

Aryl boronic acid, Suzuki-Miyaura reaction

Aryl continuous-flow Suzuki-Miyaura

Aryl derivatives Suzuki-Miyaura reaction

Arylation Suzuki-Miyaura

Arylboronic in Suzuki-Miyaura reaction

Asymmetric Suzuki-Miyaura coupling reactions

Asymmetric synthesis Suzuki-Miyaura reaction

B-alkyl Suzuki-Miyaura

B-alkyl Suzuki-Miyaura cross-coupling

B-alkyl Suzuki-Miyaura cross-coupling reaction

Biaryl phosphines, Suzuki-Miyaura

Biaryl phosphines, Suzuki-Miyaura coupling

Boronic acids Suzuki-Miyaura reaction

By Suzuki-Miyaura biaryl

Carbon Suzuki-Miyaura coupling

Carbon Suzuki-Miyaura coupling reaction

Catalysis Suzuki-Miyaura coupling

Catalyst-transfer Suzuki-Miyaura coupling

Chapter Suzuki-Miyaura Coupling

Coupling, organometallic Suzuki-Miyaura

Cross-coupling reactions Suzuki-Miyaura reaction

Direct Suzuki-Miyaura type reaction

Enantioselectivity Suzuki-Miyaura coupling

Hayashi-Miyaura reaction

Hayashi-Miyaura reaction chiral ligands

Heck-Mizoroki/Suzuki-Miyaura domino reaction

Hosomi-Miyaura borylation

Intramolecular Suzuki-Miyaura coupling

Metal Suzuki-Miyaura cross-coupling

Microreactor Suzuki-Miyaura reaction

Microwave-assisted Suzuki-Miyaura

Microwave-assisted Suzuki-Miyaura coupling

Microwave-assisted reactions Suzuki-Miyaura reaction

Miyaura boration

Miyaura boration reaction

Miyaura boronic ester synthesis

Miyaura borylation

Miyaura borylation reaction

Miyaura reaction

Miyaura reaction esters

NHC-Ni-catalyzed Suzuki-Miyaura and Negishi Cross-couplings

Nickel catalyzed cross Suzuki-Miyaura coupling

Palladium Suzuki-Miyaura cross-coupling

Palladium catalysis Suzuki-Miyaura

Palladium catalysis Suzuki-Miyaura reaction

Palladium catalysts Suzuki-Miyaura coupling

Palladium-catalyzed Suzuki-Miyaura Cross-coupling Reactions of Functionalized Aryl and Heteroaryl Boronic Esters

Palladium-promoted reaction Suzuki-Miyaura

Pd-catalysed Suzuki-Miyaura cross-coupling

Phenylboronic acid, Suzuki-Miyaura cross-coupling

Phosphine ligands Suzuki-Miyaura reaction

Pyrimidines, Suzuki-Miyaura

Pyrimidines, Suzuki-Miyaura coupling

Reactions with Organoboron Reagents The Suzuki-Miyaura Reaction

Room temperature reactions Suzuki-Miyaura coupling

Stille reaction Suzuki -Miyaura/direct

Suzuki Miyaura aryl chlorides

Suzuki Miyaura biaryls

Suzuki Miyaura chiral biaryls

Suzuki Miyaura sterically hindered substrates

Suzuki-Miyaura

Suzuki-Miyaura conditions

Suzuki-Miyaura coupling

Suzuki-Miyaura coupling Subject

Suzuki-Miyaura coupling advances

Suzuki-Miyaura coupling advantages

Suzuki-Miyaura coupling alkenylboranes

Suzuki-Miyaura coupling alkylboranes

Suzuki-Miyaura coupling asymmetric

Suzuki-Miyaura coupling bases

Suzuki-Miyaura coupling boronate species

Suzuki-Miyaura coupling catalysts

Suzuki-Miyaura coupling catalytic cycle

Suzuki-Miyaura coupling centers

Suzuki-Miyaura coupling chemistry

Suzuki-Miyaura coupling enantioselective

Suzuki-Miyaura coupling generation

Suzuki-Miyaura coupling ligands

Suzuki-Miyaura coupling optimal reaction conditions

Suzuki-Miyaura coupling partners

Suzuki-Miyaura coupling products

Suzuki-Miyaura coupling reaction conditions

Suzuki-Miyaura coupling reaction synthesis

Suzuki-Miyaura coupling reactions

Suzuki-Miyaura coupling reactions ligand

Suzuki-Miyaura coupling reactions vinyl bromides

Suzuki-Miyaura coupling scheme

Suzuki-Miyaura coupling side reactions

Suzuki-Miyaura coupling solvents

Suzuki-Miyaura coupling stereochemistry

Suzuki-Miyaura coupling synthesis

Suzuki-Miyaura coupling systems

Suzuki-Miyaura coupling water

Suzuki-Miyaura coupling with palladium carbenes

Suzuki-Miyaura cross coupling

Suzuki-Miyaura cross-coupling conditions

Suzuki-Miyaura cross-coupling ligands

Suzuki-Miyaura cross-coupling pinacolborane

Suzuki-Miyaura cross-coupling reaction

Suzuki-Miyaura crosscoupling

Suzuki-Miyaura reaction

Suzuki-Miyaura reaction application

Suzuki-Miyaura reaction catalysts

Suzuki-Miyaura reaction copper catalysts

Suzuki-Miyaura reaction mechanism

Suzuki-Miyaura reaction methodology

Suzuki-Miyaura reaction nickel catalysts

Suzuki-Miyaura reaction palladium

Suzuki-Miyaura reaction palladium-catalyzed

Suzuki-Miyaura reaction rhodium catalysts

Suzuki-Miyaura reaction synthetic application

Suzuki-Miyaura reaction trifluoroborates

Suzuki-Miyaura reaction, aqueous palladium

Suzuki-Miyaura reactions, with

Suzuki-Miyaura synthesis of biaryls

Suzuki-Miyaura, Ullmann, Sonogashira, and Heck Coupling Reactions

Suzuki-Miyaura-type

The Suzuki-Miyaura Coupling

The Suzuki-Miyaura Reaction

The Suzuki-Miyaura cross-coupling reaction

Transition metal catalysts Suzuki-Miyaura reaction

Transmetallation in the Suzuki-Miyaura Reaction

Water-based reactions Suzuki-Miyaura reaction

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