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- W2331511013 endingPage "923" @default.
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- W2331511013 abstract "A new strategy for the synthesis of 2-aminobenzimidazol-6-ols via a reaction of quinones with guanidine derivatives is reported. Sequential application of this methodology provided a simple access to the first benzosceptrin analogue bearing a bis-2-aminoimidazole moiety. A concomitant addition of two guanidines to the naphtho[1′,2′:4,5]imidazo[1,2-a]pyrimidine-5,6-dione, which includes the redox neutral debenzylation and guanidine-assisted cleavage of the 2-aminopyrimidine part resulted in the synthesis of the free challenging contiguous bis-2-aminoimidazole moiety of benzosceprins in one step." @default.
- W2331511013 created "2016-06-24" @default.
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- W2331511013 date "2014-01-30" @default.
- W2331511013 modified "2023-09-25" @default.
- W2331511013 title "Reaction of Quinones and Guanidine Derivatives: Simple Access to Bis-2-aminobenzimidazole Moiety of Benzosceptrin and Other Benzazole Motifs" @default.
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- W2331511013 doi "https://doi.org/10.1021/ol403672p" @default.
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