| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273587 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
Arenamide A and its diastereomer have been synthesized in a convergent fashion. The key steps involved in this synthesis are Sharpless asymmetric epoxidation, C-C bond formation, and macrolactamization.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
S. Chandrasekhar, G. Pavankumarreddy, K. Sathish,