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pubmed-article:12423116pubmed:abstractTextPd(OAc)(2):pyridine (1:4) is an efficient catalyst system for the oxidation of alcohols with molecular oxygen. A mechanistic study of this reaction reveals that pyridine promotes the aerobic oxidation of palladium(0) but inhibits the oxidation of alcohol by palladium(II). Kinetic results reveal that turnover-limiting substrate oxidation consists of (i) formation of a palladium(II)-alkoxide, (ii) pyridine dissociation, and (iii) beta-hydride elimination. These results provide a framework for the design and/or screening of more effective aerobic oxidation catalysts.lld:pubmed
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pubmed-article:12423116pubmed:authorpubmed-author:SteinhoffBrad...lld:pubmed
pubmed-article:12423116pubmed:authorpubmed-author:StahlShannon...lld:pubmed
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pubmed-article:12423116pubmed:pagination4179-81lld:pubmed
pubmed-article:12423116pubmed:dateRevised2003-11-3lld:pubmed
pubmed-article:12423116pubmed:year2002lld:pubmed
pubmed-article:12423116pubmed:articleTitleLigand-modulated palladium oxidation catalysis: mechanistic insights into aerobic alcohol oxidation with the Pd(OAc)(2)/pyridine catalyst system.lld:pubmed
pubmed-article:12423116pubmed:affiliationDepartment of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, WI 53706, USA.lld:pubmed
pubmed-article:12423116pubmed:publicationTypeJournal Articlelld:pubmed
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