An electrochemical emulsion microenvironment enables TEMPO-mediated selective oxidation of alcohols to aldehydes with high selectivity and broad substrate scope.

Betaine, a renewable and biodegradable osmolyte, is a biogenic option for sustainable solvents. Deep eutectic solvents allow high substrate loading and enhance biocatalysis. MD simulations guide green solvent design.

A new two-step route, i.e. , p -toluidine first reacted with dimethyl carbonate to form metholylcarbamate (MTCM), and then MTCM further converted to amino-methyl- N -phenylcarbamate (TMC), was realized in this work.

We report here the continuous flow synthesis of a high-value sugar nucleotide. Immobilisation of enzymes onto solid carriers permitted transfer of the biocatalysts into packed bed reactors to realise a continuous biocatalytic platform for the synthesis of uridine diphosphate N-acetylglucosamine (UDP-GlcNAc) on 100 mg scale, with capacity for multiple reuses. The modular continuous flow approach described here represents a significant, up to 11-fold, improvement in space time yield (STY) when compared to batch studies, along with preventing product induced enzyme inhibition, reducing the need for an additional enzyme to break down inorganic pyrophosphate (PPi). The modular nature of the system has also allowed tailored conditions to be applied to each enzyme, overcoming issues relating to thermal stability. This development presents a platform approach towards a more efficient, continuous synthesis of important glycan targets including glycoproteins, specific oligosaccharide sequences and glycosylated drug targets.

Biothiol-degradable silica nanocomposites (pf-ReSiNPs) with encapsulated rose bengal were synthesized in flow, facilitating organodisulfide synthesis with the benefit of easy recycling.

Computer-assisted methods, which hold the promise to transform synthetic organic chemistry, are often limited by experimental data lacking in quality, diversity, and quantity. In solid-phase peptide synthesis (SPPS), automated flow chemistry is well-suited to deliver such data, which is key for prediction and optimization of sequence-dependent “difficult couplings”, and insights obtained in flow-SPPS can be transferred to batch-SPPS. The current data analysis techniques rely on the height and the width of fluorenylmethoxycarbonyl (Fmoc) deprotection peaks and perform well under standard conditions. Yet any deviation in parameters (e.g. temperature, flow rate, resin loading) leads to incomplete capture of information and exclusion from the dataset. Here, we present a flexible and robust processing and analysis method that is based on the Gaussian shape of the deprotection peaks to overcome these challenges, which drastically increases the interpretable size of our data set. Using this straightforward method retains the full information and data quality while the generation of hazardous dimethylformamide solvent waste is reduced by 50%. Overall, this work highlights how the interplay between synthetic and computational analysis enables the collection of high-quality data even under non-ideal, non-standard conditions.

Selective catalytic reduction of NOx by NH3 is an emerging technology for emission control applications worldwide. The development of structured catalysts for process intensification is of growing interest in catalytic...

Non-oxidative methane coupling in an atmospheric pressure plasma jet reactor with an internal diameter of 3.0 mm has been studied. The jet reactor consisted of a quartz tube surrounded by a copper ring and a stainless-steel tube, which were separated by a variable distance. The stainless-steel tube (inner diameter: 1.0 mm, outer diameter: 1.5 mm) served as high voltage electrode and gas inlet. The jet characteristics with different tip angles of the high voltage electrode were investigated using voltage–current waveforms and gas analysis at a constant methane flow rate of 100 ml min−1. The effect of the length of the ground electrode and the gap between the electrodes on conversion, C2 selectivity and energy efficiency has been studied. The methane conversion was nearly tripled with a sharp angle of the electrode (15°), while the energy consumption was reduced from 150 to 55 kJ molC2Hy−1. The carbon deposition was also reduced.

The use of biologics in positron emission tomography (PET) imaging is an important area of radiopharmaceutical development and new automated methods are required to facilitate their production. We report an automated radiosynthesis method to produce a radiolabelled biologic via facile inverse electron demand Diels–Alder (IEDDA) “click” chemistry on a single GE FASTLab™ cassette. We exemplified the method by producing a fluorine-18 radiolabelled interleukin-2 (IL2) radioconjugate from a trans-cyclooctene (TCO) modified IL2 precursor. The radioconjugate was produced using a fully automated radiosynthesis on a single FASTLab™ cassette in a decay-corrected radiochemical yield (RCY, d.c.) of 19.8 ± 2.6% in 110 min (from start of synthesis); the molar activity was 132.3 ± 14.6 GBq μmol−1. The in vitro uptake of [18F]TTCO-IL2 correlated with the differential receptor expression (CD25, CD122, CD132) in PC3, NK-92 and activated human PBMCs. The automated method may be adapted for the radiosynthesis of any TCO-modified protein via IEDDA chemistry.