摘要
A convergent access to substituted 2-iminoimida-zolidines from aromatic amines andN-propargylS-methylthioureais developed via Ag(I)-mediated cascade guanylation-cyclizationreactions. This method features high regioselectivity, excellentefficiency, and mild reaction conditions. Subsequent deprotectionof the Boc (tert-butyloxycarbonyl) group under acidic conditionsprovides expedient access to aryl 2-aminoimidazole derivatives in aconvenient manner.
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单位1; 广州中医药大学