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杂环化合物是许多天然产物和药物的重要骨架。因此，发展杂环化合物的新合成方法一直是合成化学的研究重点和热点。但已报道的方法大多存在原子经济性和步骤经济性问题，并且需要当量的酸或碱。我们利用C-H氧化官能团化策略，高原子和步骤经济性的合成一系列杂环化合物及其重要药物骨架(Scheme 1)。
Synthesis of Heterocycles via C-H Oxidative Radical Functionalization
【摘 要】
：
杂环化合物是许多天然产物和药物的重要骨架。因此，发展杂环化合物的新合成方法一直是合成化学的研究重点和热点。但已报道的方法大多存在原子经济性和步骤经济性问题，并且
【机 构】
：
KeyLaboratoryofJiangxiProvinceforPersistentPollutantsControlandResourcesRecycle,NanchangHangkongUniv
【出 处】
：
中国化学会第十三届全国有机合成化学学术研讨会
【发表日期】
：
2016年10期
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