| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5265397 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
Here we report a two-step preparation protocol of α-benzoyloxyalkylzinc bromides from α-benzoyloxyalkyl selenides, and their application to palladium-catalyzed cross-coupling reactions with aryl and vinyl iodides. The developed method effectively provides a variety of benzoyl-protected benzylic and allylic alcohol derivatives through the formation of C(sp3)-C(sp2) bonds without affecting various polar functional groups.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Komei Sakata, Daisuke Urabe, Masayuki Inoue,