Related Experiment Video
Updated: Nov 9, 2025

Continuous Flow Chemistry: Reaction of Diphenyldiazomethane with p-Nitrobenzoic Acid
Published on: November 15, 2017
Development of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic
Ashley P Mattey1, Grayson J Ford1, Joan Citoler1
1Manchester Institute of Biotechnology (MIB) &, School of Chemistry, The University of Manchester, 131 Princess Street, Manchester, M1 7DN, UK.
Abstract:
A key aim of biocatalysis is to mimic the ability of eukaryotic cells to carry out multistep cascades in a controlled and selective way. As biocatalytic cascades get more complex, reactions become unattainable under typical batch conditions. Here a number of continuous flow systems were used to overcome batch incompatibility, thus allowing for successful biocatalytic cascades. As proof-of-principle, reactive carbonyl intermediates were generated in situ using alcohol oxidases, then passed directly to a series of packed-bed modules containing different aminating biocatalysts which accordingly produced a range of structurally distinct amines. The method was expanded to employ a batch incompatible sequential amination cascade via an oxidase/transaminase/imine reductase sequence, introducing different amine reagents at each step without cross-reactivity. The combined approaches allowed for the biocatalytic synthesis of the natural product 4O-methylnorbelladine.
Related Concept Videos
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Overview
Preparation of Amines: Reductive Amination of Aldehydes and Ketones
Aldehydes and Ketones with Amines: Imine and Enamine Formation Overview
Amino Acid Biosynthetic Pathways
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...

