Enantioselective Formal Synthesis of Palmerolide A
| Data(s) |
2011
|
|---|---|
| Resumo |
Enantioselective formal synthesis of macrolactone palmerolide A, a polyketide marine natural product, is described. Key strategies in the synthesis include the oxidative furan ring-opening of a chiral furyl carbinol for the installation of the 1,4-dienol core and a Jung nonaldol-aldol reaction for the dienamide core. |
| Formato |
application/pdf application/pdf |
| Identificador |
http://eprints.iisc.ernet.in/40447/1/Enantioselective.pdf http://eprints.iisc.ernet.in/40447/2/Supporting_information.pdf Prasad, Kavirayani R and Pawar, Amit B (2011) Enantioselective Formal Synthesis of Palmerolide A. In: Organic Letters, 13 (16). pp. 4252-4255. |
| Publicador |
American Chemical Society |
| Relação |
http://eprints.iisc.ernet.in/40447/ |
| Palavras-Chave | #Organic Chemistry |
| Tipo |
Journal Article PeerReviewed |
