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Microwave Chemistry: Cross-Coupling of Acyl Chlorides, Synthesis of Tertiary Amides, Indole-Fused 1,4-Diazepines, and Aristolactams
... and acetophenone derivatives via the Suzuki-type cross-coupling of aromatic and ... Chemical Technology have published a Suzuki-Miayura coupling / aldol condensation ... Dallinger Karl-Franzens-University Graz Palladium-Phosphinous Acid-Catalyzed Cross-Coupling of Acyl Chlorides The ...
URL: https://www.organic-chemistry.org/Highlights/2008/15SeptemberB.shtm
Triazole-Based Monophosphine Ligands for Palladium-Catalyzed Cross-Coupling Reactions of Aryl Chlorides
... ,2 ,3-Triazoles , Suzuki Coupling , Buchwald-Hartwig Coupling ... yields in amination reactions and Suzuki-Miyaura coupling reactions of unactivated ... Triazole-Based Monophosphine Ligands for Palladium-Catalyzed Cross-Coupling Reactions of Aryl Chlorides ...
URL: https://www.organic-chemistry.org/abstracts/lit1/250.shtm
Stereoconvergent Amine-Directed Alkyl-Alkyl Suzuki Reactions of Unactivated Secondary Alkyl Chlorides
... Chemistry Portal Stereoconvergent Amine-Directed Alkyl-Alkyl Suzuki Reactions of Unactivated Secondary ... stereoconvergent, arylamine-directed alkyl-alkyl Suzuki cross-coupling reactions, structure-enantioselectivity studies ... 5794-5797. Key Words Suzuki Coupling , Alkyl-Alkyl Coupling , ...
URL: https://www.organic-chemistry.org/abstracts/lit3/288.shtm
Applications of ?-Phosphonovinyl Tosylates in the Synthesis of ?-Arylethenylphosphonates via Suzuki-Miyaura Cross-Coupling Reactions
... Words alkenylation , phosphonates , Suzuki coupling ID: J54-Y2015 ... the Synthesis of ?-Arylethenylphosphonates via Suzuki-Miyaura Cross-Coupling Reactions Yewen Fang ... , Li Zhang, Jinjian Li, Xiaoping Jin* ...
URL: https://www.organic-chemistry.org/abstracts/lit4/824.shtm
C2-Symmetric Bis-Hydrazones as Ligands in the Asymmetric Suzuki-Miyaura Cross-Coupling
... for more examples Key Words Suzuki Coupling , Biaryls ID ... as Ligands in the Asymmetric Suzuki-Miyaura Cross-Coupling Antonio Bermejo, ... Ros, Rosario Fernández and José M. Lassaletta* ...
URL: https://www.organic-chemistry.org/abstracts/lit2/351.shtm
A Highly Active Catalyst for Suzuki-Miyaura Cross-Coupling Reactions of Heteroaryl Compounds
... for more examples Key Words Suzuki Coupling , Heterobiaryls ID ... A Highly Active Catalyst for Suzuki-Miyaura Cross-Coupling Reactions of Heteroaryl ... Kelvin L. Billingsley, Kevin W. Anderson, ...
URL: https://www.organic-chemistry.org/abstracts/lit1/254.shtm
Solvent-Free Microwave-Assisted Suzuki-Miyaura Coupling Catalyzed by PEPPSI-iPr
... Abstract Microwave activation enables a Suzuki coupling of boronic acids ... Organic Chemistry Portal Solvent-Free Microwave-Assisted Suzuki-Miyaura Coupling Catalyzed by PEPPSI-iPr ... biaryls , green chemistry , cross-coupling ID: J60-Y2009-1980 ...
URL: https://www.organic-chemistry.org/abstracts/lit2/588.shtm
Highly E-Selective, Stereoconvergent Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling of Alkenyl Ethers
... Key Words styrene derivatives , Suzuki coupling ID: J54-Y2019 ... Highly E-Selective, Stereoconvergent Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling of Alkenyl Ethers ... Ho, Heiko Sommer, Ilan Marek* *Schulich ...
URL: https://www.organic-chemistry.org/abstracts/lit6/809.shtm
Facile Synthesis of Highly Stable Gold Nanoparticles and Their Unexpected Excellent Catalytic Activity for Suzuki-Miyaura Cross-Coupling Reaction in Water
... for more exampels Key Words Suzuki Coupling , Biaryls , ... Unexpected Excellent Catalytic Activity for Suzuki-Miyaura Cross-Coupling Reaction in Water ... Han, Yan Liu and Rong Guo* *School ...
URL: https://www.organic-chemistry.org/abstracts/lit2/455.shtm
Suzuki-Miyaura Cross-Couplings Mediated by trans-PdBr(N-Succ)(PPh3)2: A Convenient Synthetic Method for Diarylmethanes and Aryl(heteroaryl)methanes
... , phosphine, diarylmethanes , Suzuki Coupling ID: J66-Y2009-0400 ... Organic Chemistry Portal Suzuki-Miyaura Cross-Couplings Mediated by trans-PdBr( ... phosphine, diarylmethanes , Suzuki Coupling ID: J66-Y2009-0400 ...
URL: https://www.organic-chemistry.org/abstracts/lit2/428.shtm
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