| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275999 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
The first enantiocontrolled total synthesis of heliespirone B has been accomplished employing a biomimetic intramolecular oxy-Michael reaction followed by the regio- and diastereoselective reduction of the carbonyl function as key steps.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
