Issue 3, 2007

Reuse of chiral cationic Pd–phosphinooxazolidine catalysts in ionic liquids: highly efficient catalytic asymmetric Diels–Alder reactions

Abstract

Chiral cationic palladium–phosphinooxazolidine catalysts in ionic liquid afforded excellent enantioselectivity in Diels–Alder reactions and the catalyst was easily recycled eight times without any significant decrease in chemical yields or enantioselectivity (89–99%, 88–99% ee).

Graphical abstract: Reuse of chiral cationic Pd–phosphinooxazolidine catalysts in ionic liquids: highly efficient catalytic asymmetric Diels–Alder reactions

Supplementary files

Article information

Article type
Communication
Submitted
03 Aug 2006
Accepted
25 Sep 2006
First published
25 Oct 2006

Chem. Commun., 2007, 263-265

Reuse of chiral cationic Pd–phosphinooxazolidine catalysts in ionic liquids: highly efficient catalytic asymmetric Diels–Alder reactions

K. Takahashi, H. Nakano and R. Fujita, Chem. Commun., 2007, 263 DOI: 10.1039/B611228E

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