Quinonoid compounds via reactions of lawsone and 2-aminonaphthoquinone with α-bromonitroalkenes and nitroallylic acetates: Structural diversity by C-ring modification and cytotoxic evaluation against cancer cells. [electronic resource]
Producer: 20180522Description: 686-704 p. digitalISSN:- 1768-3254
- Acetates -- chemical synthesis
- Alkenes -- chemical synthesis
- Amination
- Antineoplastic Agents -- chemical synthesis
- Cell Line, Tumor
- Chemistry Techniques, Synthetic
- Furans -- chemical synthesis
- Halogenation
- Humans
- Models, Molecular
- Naphthoquinones -- chemical synthesis
- Neoplasms -- drug therapy
- Pyrroles -- chemical synthesis
- Quinones -- chemical synthesis
- Structure-Activity Relationship
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Publication Type: Journal Article
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