| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279930 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
An efficient synthesis of trans-α-methylene-γ-butyrolactones is disclosed from syn-homoallylic alcohols via the intramolecular mesylate displacement reaction promoted by nearby ester group under the influence of MsCl/Et3N. syn-Homoallylic alcohols were prepared via the In-mediated Barbier reaction of the bromides of Baylis-Hillman adducts.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bo Ram Park, Ko Hoon Kim, Jae Nyoung Kim,