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Scope of palladium-catalyzed alkylative ring opening.
Lautens, Mark; Hiebert, Sheldon.
Afiliação
  • Lautens M; Department of Chemistry, University of Toronto, Toronto, Ontario, Canada M5S 3H6. mlautens@chem.utoronto.ca
J Am Chem Soc ; 126(5): 1437-47, 2004 Feb 11.
Article em En | MEDLINE | ID: mdl-14759202
ABSTRACT
We have explored the scope of the palladium-catalyzed nucleophilic ring opening methodology. New highly selective and highly active catalysts have been found for the ring opening of oxabenzonorbornadienes. Employing these catalysts, the addition of various alkyl nucleophiles to oxabenzonorbornadiene has been achieved. In addition, reaction of diethylzinc with [3.2.1] oxabicyclic alkenes has been accomplished to yield ring-opened products as well as functionalized alkene addition products.
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Base de dados: MEDLINE Idioma: En Ano de publicação: 2004 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Idioma: En Ano de publicação: 2004 Tipo de documento: Article