Abstract
AbstractA novel synthetic method for the formation of thiazolo[4,5‐b]indol‐2‐amines from α‐diazoimidamides and mono‐substituted thioureas in the presence of a catalytic amount of boron trifluoride etherate and camphorsulfonic acid under mild conditions was demonstrated. This methodology has a wide‐ranging scope of α‐diazoimidamides and mono‐substituted thioureas, amenable for upscaling experiments and further transformation.
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