The first example of a kinetic resolution via chlorofunctionalization of olefins is reported. The enantiomers of racemic unsaturated amides were found to have different hydrogen bonding affinities for chiral Lewis bases in numerous solvents. This interaction was exploited in developing a kinetic resolution of racemic unsaturated amides via halocyclization. The same catalyst serves to both "sense chirality" in the delivery onto the olefin functionality, resulting in stereotriad substrate as well as mediate a highly face-selective chlorine products in up to 99:1 dr and up to 98.5:1.5 er. The selectivity factors were typically greater than 50 to allow for the simultaneous synthesis of both the products and unreacted substrates in highly enantio enriched form at yields approaching 50%. The reaction employs catalytic amounts (<= 0.50 mol %) of a commercially available and recyclable organocatalyst.