Orientational Chirality, Its Asymmetric Control, and Computational Study

Abstract

Orientational chirality was discovered and characterized by a C(sp)–C(sp 3 ) axis-anchored chiral center and a remotely anchored blocker. X-ray structural analysis proved that orientatiomers are stabilized by through-space functional groups, making it possible for 1 R - or S -chiral center to exhibit 3 orientational isomers simply by rotating operations. A new model system was proposed, fundamentally different from the traditional Felkin–Ahn-type or Cram-type models. In these traditional models, chiral C(sp 3 ) center and blocking C(sp 2 ) carbons are connected adjacently, and there exist 6 energy barriers during rotating along the C(sp 2 )−C(sp 3 ) axis. In comparison, the present orientational chirality model shows that a chiral C(sp)–C(sp 3 ) carbon is remotely located from a blocking group. Thus, it is focused on the steric dialog between a chiral C(sp 3 ) center and a remotely anchored functional group. There exist 3 energy barriers for either ( R )– or ( S )–C(sp)–C(sp 3 ) stereogenicity in the new model. Chiral amide auxiliary was proven to be an excellent chiral auxiliary in controlling rotations of orientatiomers to give complete stereoselectivity. The asymmetric synthesis of individual orientatiomers was conducted via multistep synthesis by taking advantage of the Suzuki–Miyaura cross-coupling and Sonogashira coupling reactions. Density functional theory computational study presented optimized conformers and relative energies for individual orientatiomers. This discovery would be anticipated to result in a new stereochemistry topic and have a broad impact on chemical, biomedical, and material sciences in the future.