Asymmetric Carbamoyl Anion Additions to Chiral <i>N</i>‑Phosphonyl Imines via the GAP Chemistry Process and Stereoselectivity Enrichments

Carbamoyl anions were found to smoothly react with chiral <i>N</i>-phosphonyl imines in toluene at −78 °C to r.t. using LiHMDS as the base. Group-assisted purification (GAP) has been utilized to give the pure amides without using column chromatography or recrystallization. The asymmetric reaction resulted in chiral <i>N</i>-phosphonyl amino amides with good to excellent yields (71–99%) and good crude diastereoselectivities (<i>dr</i> 84:16–95:5). In this GAP procedure, the crude solids are washed with diethyl ether to afford the pure products, as revealed by ¹H NMR analysis; GAP washing consistently increases the diastereopurity of the products, resulting in excellent diastereoselectivities, often with final <i>dr</i> > 99:1. Interestingly, the diastereoenriched products can be obtained either in the ether solution or as the suspended solid, depending on the substrate