PhICl(2)-Mediated Regioselective and Electrophilic Oxythio/Selenocyanation of o-(1-Alkynyl)benzoates: Access to Biologically Active S/SeCN-Containing Isocoumarins

PhICl(2)介导的邻(1-炔基)苯甲酸酯的区域选择性亲电氧硫/硒氰化反应:合成具有生物活性的含S/SeCN基团的异香豆素

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Abstract

The application of PhICl(2)/NH(4)SCN and PhICl(2)/KSeCN reagent systems to the synthesis of the biologically active S/SeCN-containing isocoumarins via a process involving thio/selenocyanation, enabled by thio/selenocyanogen chloride generated in situ, followed with an intramolecular lactonization was realized. Gram-scale synthesis, further derivatization to access C4 thio/selenocyanated Xyridin A and anti-tumor activities of the obtained products highlight the potential use of this method.

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