Enantioselective Rearrangement Coupled with Water Addition: Direct Synthesis of Enantiomerically Pure Saturated Carboxylic Acids from α,β-Unsaturated Aldehydes

A novel type of organic synthesis enabling a direct one‐pot transformation of α,β‐unsaturated aldehydes into saturated carboxylic acids is described. As sole reagent water is required, which is integrated completely in the product. This tandem process proceeds under perfect atom economy, and consists of two coupled redox biotransformations without the need of external co‐substrates for cofactor regeneration. The initial reduction of the CC double bond of an α,β‐unsaturated aldehyde is catalyzed by an NADPH‐dependent ene reductase, leading to the formation of the saturated aldehyde and NADP+. The aldehyde intermediate is then oxidized to the corresponding carboxylic acid, thus regenerating NADPH for the next catalytic cycle. When using prochiral α,β‐unsaturated aldehydes as substrates the corresponding carboxylic acids are formed enantioselectively with up to >99 % ee as demonstrated, e.g., for the transformation of citral to (S)‐citronellic acid. Making a splash with citral: The direct one‐pot transformation of α,β‐unsaturated aldehydes to saturated carboxylic acids using only water proceeds with perfect atom economy. This tandem process involves two redox biotransformations without need of additional external co‐substrates for cofactor regeneration. With, for example, citral as prochiral α,β‐unsaturated aldehyde, transformation to (S)‐citronellic acid proceeds with >99 % conversion and >99 % ee.