| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271896 | Tetrahedron Letters | 2013 | 6 Pages |
Abstract
A palladium-catalyzed chelation-controlled oxidative arylation of α-methylene-γ-butyrolactones with arenes provided 3-arylmethylbutenolides as major products along with a low yield of α-arylidene-γ-butyrolactones. The selectivity might be due to a chelation between the palladium center and a directing group at the γ-position of α-methylene-γ-butyrolactones.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Se Hee Kim, Ko Hoon Kim, Hyun Ju Lee, Jae Nyoung Kim,