Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5275296 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
The total synthesis of (R)-kavain and of the C1-C6 fragment of jerangolid D has been achieved in nine and seven steps, respectively, from commercially available dimethyl d-malate. A metathesis reaction of vinyl ethers and a sulfoxide-modified Julia olefination have been employed as the key steps.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
JiÅÃ PospÃÅ¡il, István E. Markó,