Zephycandidine A, the First Naturally Occurring Imidazo[1,2-f]phenanthridine Alkaloid from Zephyranthes candida, Exhibits Significant Anti-tumor and Anti-acetylcholinesterase Activities
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Specific Targeting of Acetylcholinesterase and Butyrylcholinesterase Recognition Sites. Rational Design of Novel, Selective, and Highly Potent Cholinesterase Inhibitors
Discovery of an imidazo-phenanthridine synthon produced in a ‘five-step one-pot reaction’ leading to a new family of heterocycles with novel physical properties
Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
Synthesis of Imidazo[1,2‑ f ]phenanthridines by Recyclable Magnetic MOF-Catalyzed Coupling and Cyclization of 2‑(2-Bromoaryl)imidazoles with Cyclohexane-1,3-diones Followed by Aromatization
Spirodesertols A and B, two highly modified spirocyclic diterpenoids with an unprecedented 6-isopropyl-3 H -spiro[benzofuran-2,1′-cyclohexane] motif from Salvia deserta
Tf2O-Promoted Morgan–Walls Reaction: From a Flexible Approach to Functionalized Phenanthridines and Quinazolines to the Short and Divergent Total Syntheses of Alkaloids
N-Tosylhydrazones as a versatile building block in C-C and C-N bond construction : cyclization and biological activities
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