4.7 Article

Synthesis of Alkylated Pyrimidines via Photoinduced Coupling Using Benzophenone as a Mediator

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JOURNAL OF ORGANIC CHEMISTRY
卷 82, 期 5, 页码 2664-2671

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AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.6b03058

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  1. Program to Disseminate Tenure Tracking System (MEXT, Japan)
  2. Astellas Foundation for Research on Metabolic Disorders

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The synthesis of alkylated pyrimidines was achieved via benzophenone-mediated photoinduced coupling between saturated heterocycles and sulfonylpyrimidines. The pyrimidine ring was selectively introduced at the nonacidic C(sp(3))-H bond proximal to heteroatoms including oxygen, nitrogen, and sulfur. This is a coupling reaction mediated solely by photoexcited benzophenone, an organic molecule, without the aid of any metallic catalysts or reagents.

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