Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10579332 | Tetrahedron: Asymmetry | 2013 | 10 Pages |
Abstract
A concise total synthesis of emericellamides A and B, two cyclic depsipeptides exhibiting antibacterial and cytotoxic activities, is reported. A Paterson anti-aldol reaction and a hydroxy directed 1,3-anti reduction were applied for construction of the polypropionate unit with the required stereochemistry in emericellamides A and B. An FDPP mediated macrolactamization was used to construct the macrocycle of emericellamides A and B.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Tapan Kumar Pradhan, Karla Mahender Reddy, Subhash Ghosh,