Access to original spirocyclic derivatives via inter- or intramolecular reaction mediated by manganese(III) acetate
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摘要
An easily reproducible protocol allowing inter- or intramolecular spirocyclization on 尾-dicarbonyl structures is described. This methodology could afford a wide variety of spirocyclic pharmacophores. As examples, highly substituted spirobenzophenanthridin-6(5H)-ones and spirolactones were synthesized. These scaffolds could be used for the design of many compounds exhibiting biological activities.

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