4.8 Article

Iodine-Mediated Multicomponent Cascade Cyclization and Sulfenylation/Selenation: Synthesis of Imidazo[2,1-a]isoquinoline Derivatives

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ORGANIC LETTERS
卷 24, 期 24, 页码 4449-4453

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c01681

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资金

  1. National Natural Science Foundation of China [21971080, 22171098, 21971079]
  2. Fundamental Research Funds for the Central Universities
  3. 111 Project [B17019]

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A novel multicomponent cascade reaction has been reported for the synthesis of imidazo[2,1-a]isoquinoline derivatives in one-pot via the construction of two C-N bonds and one C-S/C-Se bond. The reaction achieves simultaneous C(sp3)-H amination and sulfenylation/selenation, avoiding complicated substrate preparation. It has simple operating conditions and good substrate compatibility.
A novel multicomponent cascade cyclization and sulfenylation/selenation using aryl methyl ketones, isoquinolin-1amine, and sodium arylsulfinates/1,2-diphenyldiselane to synthesize imidazo[2,1-a]isoquinoline derivatives in one-pot via the construction of two C-N bonds and one C-S/C-Se bond has been reported. This multicomponent reaction realizes simultaneous C(sp3)-H amination and sulfenylation/selenation, avoiding complicated prior substrate preparation. This process has simple operating conditions and good substrate compatibility.

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