A palladium-promoted oxidative annulation reaction for the synthesis of structurally diverse naphthoquinone-containing heterocycles has been developed, providing switchable access to 1,2-naphthofuroquinones and densely functionalized cyclobutene-fused 1,4-naphthofuroquinones by selective enol/enolate-directed processes. The synthetic application was extended by late-stage functionalization of an anti-HIV
已经开发了用于合成结构多样的含
萘醌的杂环的
钯促进的氧化环化反应,通过选择性的烯醇/烯醇酸酯定向方法提供了可转换的途径来接近1,2-
萘呋喃醌和稠密官能化的
环丁烯稠合的1,4-
萘呋喃醌。合成的应用通过抗HIV药物的后期功能化得以扩展。1,2-
萘呋喃醌合成的实用价值在内皮保护性先导化合物的开发中得到了强调。