Total synthesis of (-)-isoavenaciolide
| Contribuinte(s) |
Universitat de Barcelona |
|---|---|
| Resumo |
An enantioselective approach to (-)-isoavenaciolide was achieved starting from 1- undecyn-3-ol. The synthesis relied upon the preparation of a chiral 4-silyloxy-2-alkenylborane by hydroboration of a protected 2,3-allenol and subsequent stereoselective addition to 2- thiophenecarboxaldehyde |
| Identificador | |
| Idioma(s) |
eng |
| Publicador |
American Chemical Society |
| Direitos |
(c) American Chemical Society , 2013 info:eu-repo/semantics/openAccess |
| Palavras-Chave | #Biomolècules #Productes naturals #Síntesi asimètrica #Medicaments antibacterians #Fungicides #Biomolecules #Natural products #Asymmetric synthesis #Antibacterial agents #Fungicides |
| Tipo |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion |
