| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277047 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
Highly stereoselective total synthesis of (+)-eudesmin, (+)-yangambin, (â)-eudesmin, and (â)-yangambin is described. This method is useful to generate the core skeleton of furofuran rings utilizing modification of Evans asymmetric aldol condensation.
Graphical abstractStereoselective total synthesis of (+)-eudesmin, (+)-yangambin, (â)-eudesmin, and (â)-yangambin is described.Download full-size image
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jae-Chul Jung, Ju-Cheun Kim, Hyung-In Moon, Oee-Sook Park,