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• W2977000688 abstract "Readily available 4-bromobenzo[ c ][2,7]naphthyridine undergoes regioselective direct ring metalation at C-5 with TMPMgCl∙LiCl at −40 °C. Quenching with various electrophiles gives a broad range of 5-substituted products, which are building blocks for the synthesis of heterocyclic natural products and analogues thereof. In combination with a Parham-type cyclization a novel approach to pyrido[4,3,2- mn ]acridones has been worked out." @default.
• W2977000688 created "2019-10-03" @default.
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• W2977000688 date "2019-09-26" @default.
• W2977000688 modified "2023-09-30" @default.
• W2977000688 title "Functionalization of 4-bromobenzo[<i>c</i>][2,7]naphthyridine via regioselective direct ring metalation. A novel approach to analogues of pyridoacridine alkaloids" @default.
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• W2977000688 doi "https://doi.org/10.3762/bjoc.15.222" @default.
• W2977000688 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6774065" @default.
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