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Suzuki-Type Coupling Reaction (suzuki-type + coupling_reaction)
Selected AbstractsRapid Microwave-Promoted Catalyst- and Solvent-Free Suzuki-Type Coupling Reaction.CHEMINFORM, Issue 46 2006Jie Yan Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Metal Catalyst Free Suzuki-Type Coupling Reaction in Water.CHEMINFORM, Issue 43 2006Jie Yan Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Rapid Microwave-Promoted Catalyst- and Base-Free Suzuki-Type Coupling Reaction in Water.CHEMINFORM, Issue 34 2006Jie Yan Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Transition-Metal-Free Suzuki-Type Coupling Reactions.CHEMINFORM, Issue 29 2003Nicholas E. Leadbeater Abstract For Abstract see ChemInform Abstract in Full Text. [source] Iodine-Catalyzed Suzuki,Miyaura Coupling Performed in AirADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 4 2009Jincheng Mao Abstract Suzuki-type coupling reactions can be performed directly in air using a catalytic system composed of iodine, potassium carbonate, and polyethylene glycol 400 (I2/K2CO3/PEG-400). Iodine was found to be an effective additive for accelerating these couplings. The methodology is also suitable for the coupling of (E)- , -bromostyene with phenylboronic acid, with retention of the double bond geometry. [source] |