| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5284460 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Two model compounds with a substitution pattern typical of vitamin E, but without ring annulation, were synthesized and oxidized. No preference for one of the two ortho-quinone methides was found, confirming that the oxidation regioselectivity is not governed by electronic substituent effects of the annulated ring.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Thomas Rosenau, Amnon Stanger,