| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5220072 | Tetrahedron | 2012 | 5 Pages |
Abstract
An enantiospecific total synthesis of polyhydroxy δ-pyrone natural product phomopsolide B is accomplished. The main feature of the synthesis is the installation of the required E-olefin by Horner-Emmons-Wordsworth reaction and the formation of the lactone involving Still-Gennari olefination followed by lactonization.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Kavirayani R. Prasad, Phaneendra Gutala,