Demonstrates high conversions and stereoselectivities in axially chiral amines, indicating efficient synthesis methods.
We report an unprecedented amine transaminase-catalyzed asymmetric transamination of 4-alkylidene cyclohexanones, affording various axially chiral alkylidene cyclohexane amines in high conversions (up to 99%) and excellent stereoselectivities (mostly between 96% and 99% ee). The synthetic prospect was underscored further by efficient preparative-scale synthesis (67-83% isolated yields) and downstream product derivatization. Molecular dynamics simulations and related mutational studies were conducted to gain insights into effective catalysis, including the rationale for the superb observed enantioselectivity.
No takes yet. Share an insight, caveat, or question.
Xu et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: