Efficient synthesis of cytotoxic pyrido[1,2-e]purines from purines employing direct C-allylation and RCM–oxidation as key steps
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Synthetic Pyridopurines Derived from Food Pyrolysis Products: Intercalation, Interactions with Membranes, Cyclodextrin Complexation, and Biological Mitogenic Properties
2. Solution Structure of 2-(Pyrido[1,2-e]purin-4-yl)amino-ethanol Intercalated in the DNA Duplex d(CGATCG)2
3. Synthesis of fused dihydropyrido[e]purines via ring closing metathesis
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1. Pyrido[1,2-e]purine: Design and Synthesis of Appropriate Inhibitory Candidates against the Main Protease of COVID-19;The Journal of Organic Chemistry;2022-02-28
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3. Pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-5-amines as Potential Cytotoxic Agents against Human Neuroblastoma;Pharmaceuticals;2021-07-30
4. Microwave-Assisted Suzuki-Miyaura and Sonogashira Coupling of 4-Chloro-2-(trifluoromethyl)pyrido[1,2-e ]purine Derivatives;European Journal of Organic Chemistry;2019-08-06
5. Diversity-Oriented Synthesis of Imidazo-Dipyridines with Anticancer Activity via the Groebke–Blackburn–Bienaymé and TBAB-Mediated Cascade Reaction in One Pot;The Journal of Organic Chemistry;2019-07-30
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