| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10580364 | Tetrahedron: Asymmetry | 2006 | 6 Pages |
Abstract
Catalytic asymmetric etherification of cycloalkenyl esters with phenolic nucleophiles was achieved in water as the sole reaction medium under heterogeneous conditions by using 2 mol % palladium of a PS-PEG resin-supported palladium-imidazoindolephosphine complex to give optically active aryl(cycloalkenyl) ethers with up to 94% ee.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Yasuhiro Uozumi, Masahiro Kimura,