Cargando…
A Striking Exception to the Chelate Model for Acyclic Diastereocontrol: Efficient Access to a Versatile Propargyl Alcohol for Chemical Synthesis
The four-step, asymmetric synthesis of a chiral propargyl alcohol 1 from (R)-pantolactone is described. A key feature of the synthesis is a diastereoselective acetylide addition to a chiral α-alkoxy-aldehyde 7, in which unusual Felkin selectivity is observed, despite the potential for chelation cont...
Autores principales: | Tlais, Sami F., Clark, Ronald J., Dudley, Gregory B. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254915/ https://www.ncbi.nlm.nih.gov/pubmed/20032887 http://dx.doi.org/10.3390/molecules14125216 |
Ejemplares similares
-
A Versatile Porous Silver-Coordinated Material for the Heterogeneous Catalysis of Chemical Conversion with Propargylic Alcohols and CO(2)
por: Yang, Lu, et al.
Publicado: (2019) -
Comparison of macrocyclic and acyclic chelators for gallium-68 radiolabelling
por: Tsionou, Maria Iris, et al.
Publicado: (2017) -
Propargyl Amines: Versatile Building Blocks in Post‐Ugi Transformations
por: Bhoraniya, Rinkal B., et al.
Publicado: (2023) -
Synthetically Versatile Nitrogen Acyclic Carbene Stabilized Gold Nanoparticles
por: Rúbio, Guilherme M. D. M., et al.
Publicado: (2020) -
Regioselective trans-Carboboration
of Propargyl Alcohols
por: Jin, Hongming, et al.
Publicado: (2019)