| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279692 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
(Z)-Phenol-substituted alkenes were produced by the palladium(0)-catalyzed reaction of propargylic oxiranes with phenols. The regio- and stereoselective addition of phenols to alkynes occurs via the formation of Ï-propargyl- and Ï-allylpalladium complexes. The phenoxy-substituted enones were produced simultaneously depending on the reaction conditions.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Masahiro Yoshida, Yukio Morishita, Masataka Ihara,