Cargando…
Synthesis of densely functionalized enantiopure indolizidines by ring-closing metathesis (RCM) of hydroxylamines from carbohydrate-derived nitrones
BACKGROUND: Indolizidine alkaloids widely occur in nature and display interesting biological activity. This is the reason for which their total synthesis as well as the synthesis of non-natural analogues still attracts the attention of many research groups. To establish new straightforward accesses...
Autores principales: | Bonanni, Marco, Marradi, Marco, Cardona, Francesca, Cicchi, Stefano, Goti, Andrea |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151072/ https://www.ncbi.nlm.nih.gov/pubmed/18076753 http://dx.doi.org/10.1186/1860-5397-3-44 |
Ejemplares similares
-
Toward a Simulation Approach for Alkene Ring-closing Metathesis: Scope and Limitations of a Model for RCM
por: Nelson, David J., et al.
Publicado: (2011) -
Low-generation dendrimers with a calixarene core and based on a chiral C(2)-symmetric pyrrolidine as iminosugar mimics
por: Marradi, Marco, et al.
Publicado: (2012) -
Addition of lithiated enol ethers to nitrones and subsequent Lewis acid induced cyclizations to enantiopure 3,6-dihydro-2H-pyrans – an approach to carbohydrate mimetics
por: Pfrengle, Fabian, et al.
Publicado: (2010) -
Supported Catalysts Useful in Ring-Closing Metathesis, Cross Metathesis, and Ring-Opening Metathesis Polymerization
por: Suriboot, Jakkrit, et al.
Publicado: (2016) -
Kinetically E-Selective Macrocyclic Ring-Closing Metathesis
por: Shen, Xiao, et al.
Publicado: (2017)