One‐Pot Multienzyme Cascades for Stereodivergent Synthesis of Tetrahydroquinolines

The tetrahydroquinoline (THQ) framework is commonly found in natural products and pharmaceutically relevant molecules. Apart from using transition metal catalysts and chiral phosphoric acids, the chiral 2‐substituted 1,2,3,4‐THQs are synthesized using amine oxidase biocatalysts. However, the use of imine reductases (IREDs) in their asymmetric synthesis remained unexplored. In the current work, IREDs are employed in telescopic multienzyme cascades to catalyze the intramolecular reductive amination leading to chiral 2‐alkyl and 2‐aryl substituted‐1,2,3,4‐tetrahydroquinolines starting from inexpensive nitroalkenones. The cascades containing NtDBR (an ene reductase), NfsB (a nitro reductase) with either Na2S2O4 or V2O5, various IREDs, and glucose dehydrogenase (for NADPH regeneration) are used to synthesize a broad range of (R)/(S)‐2‐alkyl‐substituted (THQs) (26 examples) with high yield (up to 93 %) and excellent ee (up to 99 %) in one‐pot. The method further facilitates the one‐pot biocatalytic synthesis of chiral 2‐aryl substituted THQs (26 examples) from amino chalcones. Lastly, the asymmetric synthesis of several (R)‐ and (S)‐THQ based intermediates of Hancock alkaloids showed the practical application of the newly developed biocatalytic cascades. The work reports the synthesis of chiral tetrahydroquinolines (THQs) through one‐pot multienzyme cascades that use up to four enzymes. This highly efficient method demonstrates the preparation of a wide range of enantiocomplementary 2‐alkyl and 2‐aryl substituted THQs in high yield with excellent enantioselectivity.