| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5266435 | Tetrahedron Letters | 2013 | 6 Pages |
Abstract
The first total synthesis of (â)-ericanone was achieved in 10 steps with a 16% overall yield from p-hydroxybenzaldehyde. Notable features of this stereocontrolled approach include a Keck allylation to install the stereocenter at C3 and a 1,5-anti aldol reaction to install the hydroxyl group at C7.
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Authors
Luiz C. Dias, Paula K. Kuroishi, Ellen C. Polo, EmÃlio C. Jr.,