Catalytic Enantioselective Alkylation of Prochiral Enolates

The asymmetric alkylation of enolates is a particularly versatile method for the construction of a-stereogenic carbonyl motifs, which are ubiquitous in synthetic chemistry. Over the past several decades, the focus has shifted to the development of new catalytic methods that depart from classical stoichiometric stereoinduction strategies (e.g., chiral auxiliaries, chiral alkali metal amide bases, chiral electrophiles, etc.). In this way, the enantioselective alkylation of prochiral enolates greatly improves the step- and redox-economy of this process, in addition to enhancing the scope and selectivity of these reactions. In this review, we summarize the origin and advancement of catalytic enantioselective enolate alkylation methods, with a directed emphasis on the union of prochiral nucleophiles with carbon-centered electrophiles for the construction of a-stereogenic carbonyl derivatives. Hence, the transformative developments for each distinct class of nucleophile (e.g., ketone enolates, ester enolates, amide enolates, etc.) are presented in a modular format to highlight the state-of-the-art methods and current limitations in each area.

Automated summary

The focus has shifted from traditional asymmetric alkylations to catalytic asymmetric enolate alkylation methods, significantly improving the economic and selective aspects of the process. By combining different nucleophiles with carbon-centered electrophiles, various α-stereogenic carbonyl derivatives can be constructed.