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Search results for: suzuki coupling

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Microwave Chemistry Highlights: Oligothiophenes via Suzuki Coupling, Sonogashira Couplings in Supramolecular Chemistry, Pd-Catalyzed Amination, Diels-Alder Cycloaddition to Nanotubes
... . Oliver Kappe Karl-Franzens-University Graz Suzuki Cross Couplings for Oligothiophene ... ) a microwave-assisted double Sonogashira-Hagihara coupling for the synthesis of ... Kappe Karl-Franzens-University Graz Suzuki Cross Couplings for Oligothiophene Synthesis A ...
URL: http://www.organic-chemistry.org/Highlights/2004/15August.shtm
N-Vinylpyridinium and -ammonium Tetrafluoroborate Salts: New Electrophilic Coupling Partners for Pd(0)-Catalyzed Suzuki Cross-Coupling Reactions
... for Pd(0 )-Catalyzed Suzuki Cross-Coupling Reactions Keith R ... Buszek* and Neil Brown *Department of Chemistry, ... Tetrafluoroborate Salts: New Electrophilic Coupling Partners for Pd( ...
URL: http://www.organic-chemistry.org/abstracts/lit1/604.shtm
An N-Heterocyclic Carbene Ligand with Flexible Steric Bulk Allows Suzuki Cross-Coupling of Sterically Hindered Aryl Chlorides at Room Temperature
... with Flexible Steric Bulk Allows Suzuki Cross-Coupling of Sterically Hindered ... Chlorides at Room Temperature Gereon Altenhoff, Richard Goddard, ... system for the room-temperature Suzuki coupling of hindered and unhindered ...
URL: http://www.organic-chemistry.org/abstracts/literature/598.shtm
Microwave Chemistry Highlights: Synthesis of 7-Azaindoles, Raney Nickel Reductions, Suzuki Coupling of Oxazoles, Pd-Catalyzed Synthesis of 2-Arylaminopyrimidines
... conventional reflux heating). Suzuki Coupling of Oxazoles The ... of Michael F. Greaney from the University of Edinburgh ... as coupling partner. Both couplings were conducted at the ...
URL: http://www.organic-chemistry.org/Highlights/2006/15July.shtm
Biphenylene-Substituted Ruthenocenylphosphine for Suzuki-Miyaura Coupling of Aryl Chlorides
... , Ayako Mori, Toshio Suzuki, Jun-ichi Sakai and ... Chemistry Portal Biphenylene-Substituted Ruthenocenylphosphine for Suzuki-Miyaura Coupling of Aryl Chlorides ... Hoshi*, Taichi Nakazawa, Ippei Saitoh, Ayako ...
URL: http://www.organic-chemistry.org/abstracts/lit2/119.shtm
The First General Palladium Catalyst for the Suzuki-Miyaura and Carbonyl Enolate Coupling of Aryl Arenesulfonates
... for more reactions Key Words Suzuki Coupling, ?-Arylation ID ... General Palladium Catalyst for the Suzuki-Miyaura and Carbonyl Enolate Coupling ... Aryl Arenesulfonates Hanh Nho Nguyen, Xiaohua Huang and Stephen ...
URL: http://www.organic-chemistry.org/abstracts/literature/154.shtm
Novel Synthetic Approaches Toward Substituted Indole Scaffolds
... intramolecular Buchwald-Hartwig C-N/intermolecular Suzuki-Miyaura C-C coupling of o-gem-dihalovinylanilines ... 8 might be used for cross-coupling reactions. The Lautens ... involving a consecutive Pd-catalyzed Sonogashira coupling followed by aminopalladation and ...
URL: http://www.organic-chemistry.org/Highlights/2006/05September.shtm
Ferrocenyl Monophosphine Ligands: Synthesis and Applications in the Suzuki-Miyaura Coupling of Aryl Chlorides
... for more examples Key Words Suzuki Coupling, Biaryls ID ... Synthesis and Applications in the Suzuki-Miyaura Coupling of Aryl Chlorides ... Baillie, Lixin Zhang and Jianliang Xiao* *Department ...
URL: http://www.organic-chemistry.org/abstracts/literature/817.shtm
Suzuki-Miyaura Coupling of Diarylmethyl Carbonates with Arylboronic Acids: A New Access to Triarylmethanes
... examples Key Words Arylation, Suzuki Coupling ID: J54-Y2008-0680 ... Organic Chemistry Portal Suzuki-Miyaura Coupling of Diarylmethyl Carbonates with ... Acids: A New Access to Triarylmethanes Jung-Yi Yu and ...
URL: http://www.organic-chemistry.org/abstracts/lit2/057.shtm
Direct Vinylation and Difluorovinylation of Arylboronic Acids Using Vinyl- and 2,2-Difluorovinyl Tosylates via the Suzuki-Miyaura Cross Coupling
... for more examples Key Words Suzuki Coupling, Vinylation ID ... ,2-Difluorovinyl Tosylates via the Suzuki-Miyaura Cross Coupling Thomas M ... Gøgsig, Lina S. Søbjerg, Anders T. ...
URL: http://www.organic-chemistry.org/abstracts/lit2/099.shtm
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