Divergent Strategy in Marine Tetracyclic Meroterpenoids Synthesis
The divergent total synthesis strategy can be successfully applied to the preparation of families of natural products using a common late-stage pluripotent intermediate. This approach is a powerful tool in organic synthesis as it offers opportunities for the efficient preparation of structurally rel...
Autors principals: | Rosales Martínez, Antonio, Rodríguez García, Ignacio Manuel, López Martínez, Josefa Leticia |
---|---|
Format: | info:eu-repo/semantics/article |
Idioma: | English |
Publicat: |
MDPI
2021
|
Matèries: | |
Accés en línia: | http://hdl.handle.net/10835/11927 https://doi.org/10.3390/md19050273 |
Ítems similars
-
A Concise Route for the Synthesis of Tetracyclic Meroterpenoids: (±)-Aureol Preparation and Mechanistic Interpretation
per: Rosales Martínez, Antonio, et al.
Publicat: (2020) -
Unifying the Synthesis of a Whole Family of Marine Meroterpenoids through a Biosynthetically Inspired Sequence of 1,2-Hydride and Methyl Shifts as Key Step
per: Rosales Martínez, Antonio, et al.
Publicat: (2023) -
Unprecedented Elimination Reactions of Cyclic Aldols: A New Biosynthetic Pathway toward the Taiwaniaquinoid Skeleton
per: Guardia, Juan J., et al.
Publicat: (2023) -
Divergent explanatory production: The relationship between resilience and creativity
per: Sánchez Hernández, Óscar, et al.
Publicat: (2016) -
Marine Terpenic Endoperoxides
per: Torres García, Irene, et al.
Publicat: (2021)