Expanding Meroterpenoid Chemical Space Via Intermolecular Trapping of Cationic Cyclization Intermediates
Saved in:
| Main Authors: | Ivan Cornu, Daniel Häussinger, Alessandro Prescimone, Konrad Tiefenbacher |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
American Chemical Society
2025-06-01
|
| Series: | JACS Au |
| Online Access: | https://doi.org/10.1021/jacsau.5c00492 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Cationic amphiphilic meroterpenoids: synthesis, antibacterial, antifungal and mutagenic activity
by: Alan Akhmedov, et al.
Published: (2024-05-01) -
Evolution of a Strategy for the Total Synthesis of the Ganoderma Meroterpenoid Ganoapplanin
by: Nicolas Müller, et al.
Published: (2025-05-01) -
Research progress on heteroterpene and meroterpenoid compounds from the Rhododendron genus and their NMR characterization and biological activity
by: Jingxin Mao, et al.
Published: (2025-07-01) -
Small gold nanoparticles for tandem cyclization/reduction and cyclization/hydroalkoxylation reactions
by: Kristína Plevová, et al.
Published: (2024-10-01) -
Expanding the chemical space of flavins with pentacyclic architecture
by: Dayeong Seo, et al.
Published: (2025-04-01)