Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5215391 | Tetrahedron | 2015 | 10 Pages |
Abstract
Total synthesis of motualevic acids A-F and (E) & (Z) geometrical isomers of antazirines has been achieved from a commercially available starting material, 1,10-decanediol. The synthesis of motualevic acid E served as a common key intermediate for the synthesis of most of these natural products. The key steps involved in this synthesis were Wittig olefination, Corey-Fuchs reaction, Neber reaction, amide coupling.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Vilas D. Kadam, Gangarajula Sudhakar,