1027223-93-3Relevant articles and documents
Pourbaix diagrams in weakly coupled systems: A case study involving acridinol and phenanthridinol pseudobases
Walpita, Janitha,Yang, Xin,Khatmullin, Renat,Luk, Hoi Ling,Hadad, Christopher M.,Glusac, Ksenija D.
, p. 204 - 208 (2016)
The thermodynamics of proton-coupled electron transfer (PCET) in weakly coupled organic pseudobases was investigated using 2,7-dimethyl-9-hydroxy-9-phenyl-10-tolyl-9,10-dihydroacridine (AcrOH) and 6-phenylphenanthridinol (PheOH) as model compounds. Pourba
PYRROLOQUINOLINE ALKALOIDS AS ANTIMALARIAL AGENTS AND PROCESS FOR THE PREPARATION THEREOF
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Page/Page column 19; 21; 23, (2013/08/28)
The patent provides novel compounds with potential anti-malarial activity and process of synthesis thereof. Further, the process for the synthesis of known antimalarial natural products marinoquinazolinone A-F, aplidiopsamine A and their potential antimal
Pd-catalyzed imine cyclization: Synthesis of antimalarial natural products aplidiopsamine A, marinoquinoline A, and their potential hybrid nclite-M1
Mahajan, Jyoti P.,Suryawanshi, Yogeshwar R.,Mhaske, Santosh B.
supporting information, p. 5804 - 5807 (2013/01/15)
Palladium-catalyzed cyclization of imines has been developed to construct the extremely rare 3H-pyrrolo[2,3-c]quinoline ring system for diversity oriented first total synthesis of antimalarial marine natural product Aplidiopsamine A as well as synthesis o