| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5224763 | Tetrahedron | 2010 | 9 Pages |
Abstract
An efficient procedure for synthesizing oxazines was developed by the palladium(0)-catalyzed intramolecular cyclization of a benzamide through a Ï-allylpalladium (II) complex. Interestingly, the diastereoselectivity of oxazine ring formation was dominantly controlled by the bulkiness of various protecting groups on the secondary alcohols.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Van-Thoai Pham, Jae-Eun Joo, Kee-Young Lee, Tai-Won Kim, Yu Mu, Won-Hun Ham,