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Library Synthesis Using 5,6,7,8-Tetrahydro-1,6-naphthyridines as Scaffolds

机译:使用5,6,7,8-四氢-1,6-萘啶作为骨架的文库合成

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摘要

The chemistry of 5,6,7,8-tetrahydro-1,6-naphthyridine scaffolds, synthesized by intramolecular cobalt-catalyzed [2 + 2 + 2] cyclizations, has been exploited for library synthesis. Urea, amide, and sulfonamide formations were used in the synthesis of a 101-membered library. Screening of the library for antituberculosis activity revealed three lead compounds.
机译:通过分子内钴催化的[2 + 2 + 2]环化合成的5,6,7,8-四氢-1,6-萘啶骨架的化学性质已用于文库合成。尿素,酰胺和磺酰胺形成物用于合成101元文库。筛选抗结核活性的文库揭示了三种先导化合物。

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