The development of a continuous flow multistep strategy for the synthesis of linear peptoids and their subsequent macrocyclization via Click chemistry is described. The central transformation of this process is an Ugi four-component reaction generating the peptidomimetic core structure. In order to avoid exposure to the often toxic and malodorous isocyanide building blocks, the continuous approach was telescoped by the dehydration of the corresponding formamide. In a concurrent operation, the highly energetic azide moiety required for the subsequent intramolecular copper-catalyzed azide-alkyne cycloaddition (Click reaction) was installed by nucleophilic substitution from a bromide precursor. All steps yielding to the linear core structures can be conveniently coupled without the need for purification steps resulting in a single process generating the desired peptidomimetics in good to excellent yields within a 25 min reaction time. The following macrocyclization was realized in a coil reactor made of copper without any additional additive. A careful process intensification study demonstrated that this transformation occurs quantitatively within 25 min at 140 °C. Depending on the resulting ring strain, either a dimeric or a monomeric form of the cyclic product was obtained.

Biodiesel (rapeseed oil methyl ester) was aged in a Rancimat device at a temperature of 110 °C and an air flow of 10 L/h. Time-resolved analyses applying gas chromatography−flame ionization detection, gas chromatography−mass spectrometry, and ion-exchange chromatography on the formation of aging products were performed. Formic and acetic acid, fatty acids with chain lengths from 5 to 18 carbon atoms, fatty acid methyl esters, and epoxides were quantified. After 12 h of aging, the concentrations of formic and acetic acid were 5600 ± 80 and 1360 ± 80 mg/kg, respectively. Fatty acid concentrations were in the range of <18−4200 mg/kg after 18 h of aging. Linoleic acid methyl ester and linolenic acid methyl ester (19 and 9.1 mass % of the non-aged fuel) were shown to be fully decomposed after 24 and 18 h of aging, respectively. After 51 h of aging, the concentration of oleic acid methyl ester (63 mass % of the non-aged fuel) decreased to 2.2 mass % and trans-epoxy stearic acid methyl ester and cis-epoxy stearic acid methyl ester reached concetrations of 5.9 and 0.7 mass %, respectively. The fuel composition shows only minor changes in early stages of aging, and a strong timely correlation of the formation of aging products with the end of the induction period of fuel was observed.

Established analytic methods for the quantification of phorbol esters (PE), which are some toxic components in Jatropha curcas L., include HPLC with UV‐detection with the commercially available phorbol myristate acetate (PMA) as internal standard or HPLC coupled with MS detection with an external calibration, mostly also with PMA. The differences in the fatty acid side chains and connection to the base structure of PMA compared to PE leads to different UV absorption and MS ionization effects and cause problems for exact quantitative measurements. In this paper, a method is presented which combines both detection types and shows differences between both results. For this purpose, an extraction routine is performed on a PE‐containing seed oil to get a PE standard in high purity, which was used for a standard addition method on two real J. curcas oil samples, derived from Ghana and Mexico. Furthermore, a detection window of ±10 ppm for the high accurate ToF‐MS detection is set to eliminate isobaric interferences from co‐eluting material. Method evaluation of inter‐ and intra‐day variance as well as the recovery rate are performed and determined. With this method a limit of detection of 62 ng mL−1 (UV) and 11 ng mL−1 (MS) can be achieved. Practical Applications: Due to the good biological and technical properties of Jatropha curcas L., its seed oil seems perfect for the application as biodiesel feedstock. The toxicity on the other hand could cause problems when converting side products from the oil production to products of higher value. With the here described method an accurate and precise analysis procedure for the quantification of the toxic compounds namely, phorbol esters, could be applied for toxicity studies or routine checks in industry which is converting plant material from J. curcas, so that no toxic material is used for example as animal feed. In this paper, an exact and robust analysis method is described for the quantification of phorbol esters (PE) in Jatropha curcas L. seed oil. This method procedure includes the extraction of PE in methanol, chromatographic separation on a reverse phase C18 HPLC column and the quantification by standard addition method. For the standard addition method a highly pure PE standard is used, which is extracted and purified by semi preparative HPLC right before the measurements. The used detector for identification and quantification is UV set at 280 nm and ESI‐ToF‐MS with a ±10 ppm mass difference of the deprotonated and formate adduct pseudo molecular ion of PE.

Phenolic antioxidants have limited solubility in biodiesel, so this research developed new antioxidants by addition of hydroquinone and catechol on unsaturated fatty acid esters, which improved significantly the oxidative stability of rapeseed biodiesel. This new compound class is more soluble in biodiesel than hydroquinone and catechol, in same molar concentrations. The aging of biodiesel was studied using Metrohm model 743 Rancimat and PetroOxy devices and it was possible to observe an improvement on oxidation stability in both testing using these new antioxidants. Especially the additives 2MB3 and 4MB3 improved the induction period (IP) of rapeseed methyl ester (RME‐B100), from 4 to 63 and 65 h, respectively, with 30 mmol/kg of additives, while hydroquinone in comparison improves the stability to 25 h in the same molar concentration. This new class of antioxidants is promising to enhance oxidative stability of biodiesel, showing the capability of such additives to be commercialized for this purpose. Practical applications: Biodiesel is obtained by different raw materials, so the composition is different according to the source. The biodiesel with higher amounts of unsaturated fatty acids is more susceptible to oxidation than those with higher saturation. To solve problems caused by oxidative deterioration of biodiesel, this research aimed to synthesize a new class of antioxidants as an alternative for preventing and minimize oxidative damage of biofuels. Rapeseed biodiesel without any addition of additive was out of specification according to EN 14214, which regulates oxidative stability greater or equal to 8 h. The additives herein obtained improved significantly the oxidation stability for rapeseed biodiesel by more than 100%.