Cargando…
Synthesis of the B-seco limonoid core scaffold
Synthetic investigations towards the structurally complex and highly decorated framework of B-seco limonoid natural products by means of a [3,3]-sigmatropic rearrangement are described. Detailed model studies reveal, that an Ireland–Claisen rearrangement can be employed to construct the central C9–C...
Autores principales: | Bruss, Hanna, Schuster, Hannah, Martinez, Rémi, Kaiser, Markus, Antonchick, Andrey P, Waldmann, Herbert |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943702/ https://www.ncbi.nlm.nih.gov/pubmed/24605139 http://dx.doi.org/10.3762/bjoc.10.15 |
Ejemplares similares
-
Anti-Differentiation Effect of B, D-Seco limonoids of Swietenia mahogani
por: Yang, Heejung, et al.
Publicado: (2017) -
Trienamine catalyzed asymmetric synthesis and biological investigation of a cytochalasin B-inspired compound collection
por: Sellstedt, Magnus, et al.
Publicado: (2016) -
Synthesis of Degraded Limonoid Analogs as New Antibacterial Scaffolds against Staphylococcus aureus
por: Ferrera-Suanzes, Marta, et al.
Publicado: (2020) -
Catalytic Enantioselective 1,3-Dipolar Cycloadditions
of Azomethine Ylides for Biology-Oriented Synthesis
por: Narayan, Rishikesh, et al.
Publicado: (2014) -
Enantioselective Synthesis of Five-Membered-Ring Atropisomers
with a Chiral Rh(III) Complex
por: Shaaban, Saad, et al.
Publicado: (2020)