Enantioselective Multifunctionalization with Rh Carbynoids

Multifunctionalization from the interception of active intermediates is an attractive synthetic strategy for the efficient construction of complex molecular scaffolds in an atom and step economic fashion. However, the design of reactions involving metal carbynoids that exhibit carbene/carbocation behavior is currently limited, and developing catalyst-controlled highly enantioselective versions poses significant challenges. In this study, we present the first asymmetric trifunctionalization reactions with rhodium carbynoids. This reaction unveils the distinctive reactivity of the carbynoid precursor, enabling it to react with simultaneously two nucleophiles and one electrophile. This process involves the formation of two distinct carbene ylides with the alcohol/carbamate and the trapping of one ylide with the imine, resulting in the formation of three new bonds. Furthermore, this strategy allows for the divergent synthesis of a wide array of beta-amino esters in high yields and exceptional enantioselectivity.

Automated summary

Multifunctionalization through the interception of active intermediates is an attractive strategy for the efficient synthesis of complex molecular structures. In this study, the first asymmetric trifunctionalization reactions with rhodium carbynoids were presented, allowing for the synthesis of a wide array of β-amino esters in high yields and exceptional enantioselectivity.