| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5268019 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
A 13-step, highly stereoselective synthesis of (â)-nakadomarin A has been achieved using the combination of a bifunctional organocatalyst controlled Michael addition, a nitro-Mannich/lactamization cascade, an alkyne ring-closing metathesis/syn-reduction, and furan/iminium ion cyclization/reduction as key steps.
Related Topics
Physical Sciences and Engineering
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Authors
Pavol Jakubec, Andrew F. Kyle, Jonás Calleja, Darren J. Dixon,