Chemical Consequences of the Mechanical Bond: A Tandem Active Template-Rearrangement Reaction

摘要

We report the unexpected discovery of a tandem active template CuAAC-rearrangement process, in which N-2 is extruded on the way to the 1,2,3-triazole product to give instead acrylamide rotaxanes. Mechanistic investigations suggest this process is dictated by the mechanical bond, which stabilizes the Cu-I-triazolide intermediate of the CuAAC reaction and diverts it down the rearrangement pathway; when no mechanical bond is formed, the CuAAC product is isolated.