Cargando…
Synthesis of the spiroketal core of integramycin
A concise synthetic strategy towards the spiroketal core of the HIV-integrase inhibitor integramycin (1) was developed. The required ketone precursor was efficiently constructed from two simple and easily accessible subunits by means of a hydrozirconation/copper catalyzed acylation reaction. The eff...
Autor principal: | Prusov, Evgeny V |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869345/ https://www.ncbi.nlm.nih.gov/pubmed/24367411 http://dx.doi.org/10.3762/bjoc.9.282 |
Ejemplares similares
-
Asymmetric Synthesis of Naturally Occuring Spiroketals
por: Raju, B. Rama, et al.
Publicado: (2008) -
Nitroalkanes as Central Reagents in the Synthesis of Spiroketals
por: Ballini, Roberto, et al.
Publicado: (2008) -
Designed Spiroketal Protein Modulation
por: Scheepstra, Marcel, et al.
Publicado: (2017) -
A simple and efficient method for the preparation of 5-hydroxy-3-acyltetramic acids
por: Trenner, Johanna, et al.
Publicado: (2015) -
A gold-catalyzed alkyne-diol cycloisomerization for the synthesis of oxygenated 5,5-spiroketals
por: Tlais, Sami F, et al.
Publicado: (2011)