| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277979 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
The first total synthesis of (±)-lagopodin A and a formal total synthesis of enokipodins A and B is described. The requisite precursors containing two vicinal quaternary carbon atoms were assembled employing Claisen rearrangement and an RCM reaction as key steps starting from 2,5-dimethoxy-4-methylacetophenone.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
A. Srikrishna, B. Vasantha Lakshmi, P.C. Ravikumar,