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- W1987412241 abstract "Benzimidazoles find a broad range of applications in material science, as well as biologically active compounds. They are sometimes difficult to prepare in regioisomerically pure form. This method uses available 2-haloanilines and primary amides as starting materials. It is a combination of the Cu(I)-catalyzed amidation with the subsequent ring closure, affording products with complete regioselectivity. This method is more economical and substantially less sensitive to the substitution pattern than similar Pd-catalyzed processes." @default.
- W1987412241 created "2016-06-24" @default.
- W1987412241 date "2008-01-23" @default.
- W1987412241 modified "2023-10-17" @default.
- W1987412241 title "Regiospecific Synthesis of N-Alkyl-benzimidazoles from o-Haloanilines" @default.
- W1987412241 doi "https://doi.org/10.1055/s-2007-992478" @default.
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