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Advances in palladium-catalyzed carbon-nitrogen bond forming processes

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dc.contributor.advisor Stephen L. Buchwald. en_US Tundel, Rachel E. (Rachel Elizabeth) en_US
dc.contributor.other Massachusetts Institute of Technology. Dept. of Chemistry. en_US 2007-02-21T13:21:22Z 2007-02-21T13:21:22Z 2006 en_US 2006 en_US
dc.description Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2006. en_US
dc.description Vita. Leaf 68 blank. en_US
dc.description Includes bibliographical references. en_US
dc.description.abstract Chapter 1. Microwave-assisted, palladium-catalyzed C-N bond-forming reactions with aryl/heteroaryl nonaflates/halides and amines using the soluble amine bases DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) or MTBD (7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene) and a catalyst system consisting of Pd2dba3 and ligands (XantPhos, 2-dicylcohexylphosphino-2',4',6'-triisopropyl-1,1 '-biphenyl (XPhos) and 2-di-tert-butylphosphino-2',4',6'-triisopropyl-1, '-biphenyl) resulted in good to excellent yields of arylamines in short reaction times. Chapter 2. Using a catalyst comprised of the bulky, electron-rich monophosphine ligand di-tert-Butyl XPhos (2-di-tert-butylphosphino-2',4',6'-triisopropyl-1,1'-biphenyl) and Pd2dba3 with sodium tert-butoxide as the base, amino heterocycles were coupled successfully with aryl/heteroaryl halides in moderate to excellent yields. en_US
dc.description.statementofresponsibility by Rachel E. Tundel. en_US
dc.format.extent 68 leaves en_US
dc.language.iso eng en_US
dc.publisher Massachusetts Institute of Technology en_US
dc.rights M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. en_US
dc.subject Chemistry. en_US
dc.title Advances in palladium-catalyzed carbon-nitrogen bond forming processes en_US
dc.type Thesis en_US S.B. en_US
dc.contributor.department Massachusetts Institute of Technology. Dept. of Chemistry. en_US
dc.identifier.oclc 77529823 en_US

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