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Hydriodic acid at high temperature reduces pyrrol to pyrrolidine (tetra-hydropyrrol), C 4 H 8 NH.
This substance easily splits out alcohol, and the ring compound then formed yields pyrrolidine on reduction by sodium in amyl alcohol solution.
An experimental and computational study of the enantioselective lithiation of N -Boc pyrrolidine using sparteine-like chiral diamines, J. Am.