يعرض 1 - 6 نتائج من 6 نتيجة بحث عن '"Tianyi Zheng"', وقت الاستعلام: 0.84s تنقيح النتائج
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    المؤلفون: Yan Zhang, Tianyi Zheng, Kun Tong, Shouyun Yu

    المصدر: Advanced Synthesis & Catalysis. 357:3681-3686

    الوصف: A regiospecific synthesis of ortho-trifluoromethylated and ortho-(fluoro)alkylated pyridine derivatives has been developed. This strategy is enabled by visible light-promoted vinyl isocyanide insertions with Umemoto’s reagent and electron-deficient bromides at room temperature. The methodology presented here provides an access to highly functionalized ortho-(fluoro)alkylated pyridine derivatives regiospecifically under mild conditions with good yields. The proposed mechanism was supported by TEMPO trapping experiments, Stern–Volmer analysis and light off/on and time profile experiments.

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    المصدر: Angewandte Chemie. 127:4127-4131

    الوصف: A unified strategy involving visible-light-induced iminyl-radical formation has been established for the construction of pyridines, quinolines, and phenanthridines from acyl oximes. With fac-[Ir(ppy)3 ] as a photoredox catalyst, the acyl oximes were converted by 1 e(-) reduction into iminyl radical intermediates, which then underwent intramolecular homolytic aromatic substitution (HAS) to give the N-containing arenes. These reactions proceeded with a broad range of substrates at room temperature in high yield. This strategy of visible-light-induced iminyl-radical formation was successfully applied to a five-step concise synthesis of benzo[c]phenanthridine alkaloids.

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    المؤلفون: Kun Tong, Shouyun Yu, Yan Zhang, Tianyi Zheng

    المصدر: ChemInform. 47

    الوصف: This regiospecific synthesis of highly functionalized pyridine derivatives proceeds via visible light-promoted radical isocyanide insertions with Umemoto′s reagent (II) or (fluoro)alkyl bromides.

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    المصدر: ChemInform. 46

    الوصف: A unified strategy involving visible-light-induced iminyl-radical formation has been established for the construction of pyridines, quinolines, and phenanthridines from acyl oximes. With fac-[Ir(ppy)3] as a photoredox catalyst, the acyl oximes were converted by 1 e− reduction into iminyl radical intermediates, which then underwent intramolecular homolytic aromatic substitution (HAS) to give the N-containing arenes. These reactions proceeded with a broad range of substrates at room temperature in high yield. This strategy of visible-light-induced iminyl-radical formation was successfully applied to a five-step concise synthesis of benzo[c]phenanthridine alkaloids.