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Search results for: suzuki coupling

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35 pages of results.
Cyrene as a Bio-Based Solvent for the Suzuki-Miyaura Cross-Coupling
... examples Key Words boron, Suzuki coupling , green chemistry ... a Bio-Based Solvent for the Suzuki-Miyaura Cross-Coupling Kirsty L. ... , Jane Murray, Craig Jamieson, Allan J. ...
URL: https://www.organic-chemistry.org/abstracts/lit6/275.shtm
Microwave Chemistry: Rh-Catalyzed C-H Arylations, Hydroformylation, Ugi Reaction and Intramolecular O-Arylation, Ni/C-Catalyzed Cross-Couplings
... Negishi (a ), Suzuki (b ), ... Barbara have performed several heterogeneous cross-coupling reactions catalyzed by nickel-in-charcoal ... (c ) and the coupling of vinyl alanes with ...
URL: https://www.organic-chemistry.org/Highlights/2006/15September.shtm
Rapid Nickel-Catalyzed Suzuki-Miyaura Cross-Couplings of Aryl Carbamates and Sulfamates Utilizing Microwave Heating
... examples Key Words Biaryls , Suzuki Coupling , Microwave Synthesis ... Organic Chemistry Portal Rapid Nickel-Catalyzed Suzuki-Miyaura Cross-Couplings of Aryl Carbamates ... Abstract High-speed and scalable nickel-catalyzed cross-coupling of arylboronic acids with ...
URL: https://www.organic-chemistry.org/abstracts/lit3/188.shtm
Overcoming the Naphthyl Requirement in Stereospecific Cross-Couplings to Form Quaternary Stereocenters
... for more examples Key Words Suzuki coupling , diarylmethanes ID ... stilbene ligand enables a stereospecific Suzuki-Miyaura cross-coupling of chiral tertiary ... carboxylates to provide challenging all-carbon diaryl quaternary stereocenters in good ...
URL: https://www.organic-chemistry.org/abstracts/lit7/965.shtm
Microwave Chemistry: N-Shifted Buflavine Analogues, N-Aryl Azacycloalkanes, SmBr2-, SmI2- and YbI2-Mediated Reactions, Continuous Flow Capillary Microreactor
... Several metal catalyst-employing reactions like Suzuki or RCM but also ... of Leuven has employed microwave-enhanced Suzuki-Miyaura cross-coupling and ring-closing metathesis ... RCM) as the key steps in the 6-step synthesis ...
URL: https://www.organic-chemistry.org/Highlights/2005/15June.shtm
Author: A. Suzuki
... Synthetic Reactions. A. Suzuki, Acc. Chem ... suzuki-a.shtm ...
URL: https://www.organic-chemistry.org/abstracts/authors/suzuki-a.shtm
Alkyl-Alkyl Suzuki Cross-Couplings of Unactivated Secondary Alkyl Halides at Room Temperature
... Organic Chemistry Portal Alkyl-Alkyl Suzuki Cross-Couplings of Unactivated Secondary ... 13662-13663. Room-Temperature Alkyl-Alkyl Suzuki Cross-Coupling of Alkyl Bromides that ... ? Hydrogens M. R. Netherton, C. ...
URL: https://www.organic-chemistry.org/abstracts/lit1/821.shtm
Room-Temperature Alkyl-Alkyl Suzuki Cross-Coupling of Alkyl Bromides that Possess ? Hydrogens
... Organic Chemistry Portal Room-Temperature Alkyl-Alkyl Suzuki Cross-Coupling of Alkyl Bromides ... Possess ? Hydrogens Matthew R. Netherton, Chaoyang Dai ... . Boronic Acids: New Coupling Partners in Room-Temperature Suzuki ...
URL: https://www.organic-chemistry.org/abstracts/lit0/256.shtm
General Method for the Suzuki-Miyaura Cross-Coupling of Primary Amide-Derived Electrophiles Enabled by [Pd(NHC)(cin)Cl] at Room Temperature
... Key Words aryl ketones , Suzuki coupling ID: J54-Y2017 ... Portal General Method for the Suzuki-Miyaura Cross-Coupling of Primary Amide-Derived ... Enabled by [Pd(NHC)(cin) ...
URL: https://www.organic-chemistry.org/abstracts/lit6/127.shtm
Amino Alcohols as Ligands for Nickel-Catalyzed Suzuki Reactions of Unactivated Alkyl Halides, Including Secondary Alkyl Chlorides, with Arylboronic Acids
... Alcohols as Ligands for Nickel-Catalyzed Suzuki Reactions of Unactivated Alkyl ... 10.1021/ja0613761 Abstract Suzuki cross-coupling reactions of an unprecedented ... . Boronic Acids: New Coupling Partners in Room-Temperature Suzuki ...
URL: https://www.organic-chemistry.org/abstracts/lit1/321.shtm
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