| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5221208 | Tetrahedron | 2010 | 12 Pages |
Abstract
An enantioselective total synthesis of aspergillides A and B has been accomplished on the basis of a unified synthetic strategy that exploits stereodivergent intramolecular oxa-conjugate cyclization and Yamaguchi macrolactonization.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
