High‐performance liquid chromatographic separations of stereoisomers of chiral basic agrochemicals with polysaccharide‐based chiral columns and polar organic mobile phases

The separation of the stereoisomers of 23 chiral basic agrochemicals was studied on six different polysaccharide‐based chiral columns in high‐performance liquid chromatography with various polar organic mobile phases. Along with the successful separation of analyte stereoisomers, emphasis was placed on the effect of the chiral selector and mobile phase composition on the elution order of stereoisomers. The interesting phenomenon of reversal of enantiomer/stereoisomer elution order function of the polysaccharide backbone (cellulose or amylose), type of derivative (carbamate or benzoate), nature, and position of the substituent(s) in the phenylcarbamate moiety (methyl or chloro) and the nature of the mobile phase was observed. For several of the analytes containing two chiral centers all four stereoisomers were resolved with at least one chiral selector/mobile phase combination.     

A Unified Continuous Flow Assembly-Line Synthesis of Highly Substituted Pyrazoles and Pyrazolines

A rapid and modular continuous flow synthesis of highly functionalized fluorinated pyrazoles and pyrazolines has been developed. Flowing fluorinated amines through sequential reactor coils mediates diazoalkane formation and [3+2] cycloaddition to generate more than 30 azoles in a telescoped fashion. Pyrazole cores are then sequentially modified through additional reactor modules performing N-alkylation and arylation, deprotection, and amidation to install broad molecular diversity in short order. Continuous flow synthesis enables the safe handling of diazoalkanes at elevated temperatures, and the use of aryl alkyne dipolarphiles under catalyst-free conditions. This assembly-line synthesis provides a flexible approach for the synthesis of agrochemicals and pharmaceuticals, as demonstrated by a four-step, telescoped synthesis of measles therapeutic, AS-136A, in a total residence time of 31.7 min (1.76 g h⁻¹).     

氯代烷烃、硫粉和氢亚磷酸酯一步合成S-烷基硫磷酸酯

S-苄基硫磷酸酯和S-烷基硫磷酸酯在农药中有着重要的应用。 本文发展了一种无需催化剂,仅在碱作用下,氯代烷烃、硫粉以及氢亚磷酸酯三组份一步生成S-烷基硫磷酸酯的绿色经济方法,该反应可以在一步反应中同时构建磷—硫键和碳—硫键。 以苄氯及衍生物、硫粉、氢亚磷酸酯在碳酸铯的促进下,室温反应,共合成了17个S-苄基硫磷酸酯,产率为70%~99%。 同时,实现了脂肪链的氯代烃、硫粉和氢亚磷酸酯的反应,在三乙胺的促进下,在空气中60 ℃反应,共合成了13个S-烷基硫磷酸酯,产率为45%~93%。 本方法在合成上和工业上将具有较好的应用前景。     

Synthesis and characterization of biodegradable multicomponent amphiphilic conetworks with tunable swelling through combination of ring‐opening polymerization and “click” chemistry method as a controlled release formulation for 2,4‐dichlorophenoxyacetic acid herbicide

Multicomponent (two, three, and four component) amphiphilic conetworks (APCNs) with tunable swelling behaviors were fabricated through the ring opening polymerization and click chemistry utilizing various combinations of azide and alkyne functionalized poly (ethylene glycol) (PEG) and poly (caprolactone) (PCL) precursors. Prepare azido‐terminated star‐shaped PCL, azido‐terminated PEG, alkyne‐terminated PEG, and propargylated pentaerythritol were characterized by hydrogen‐1 proton nuclear magnetic resonance (¹H NMR) and Fourier‐transform infrared (FT‐IR) spectroscopy. The morphology and thermal behavior of the APCNs were studied by scanning electron microscopy (SEM) and differential scanning calorimetry (DSC). The swelling behavior of APCNs could be manipulated through an establishment of a balance between hydrophilic segments, hydrophobic segments, and cross‐linking density. The 2,4‐dichlorophenoxyacetic acid (2,4‐D) herbicide was entrapped in APCNs as a model agrochemical to study the release profile from APCNs. The obtained results showed that the release of 2,4‐D could be controlled by the swelling degree of APCNs. Finally, the biodegradability rates of APCNs were investigated in agricultural soil. The results exhibited that the decrease in the swelling degree led to decreased degradation rate of APCNs. According to obtained results, these APCNs could be used as biomaterials for the controlled release of agrochemicals.     

Amphiphilic fluorous random copolymer self‐assembly for encapsulation of a fluorinated agrochemical

Amphiphilic self‐folding random copolymers exhibit different solution behaviors depending on the identity of the hydrophobic/hydrophilic units. Herein, it is demonstrated that changing the hydrophilic unit from poly(ethylene glycol) to the sugar trehalose causes increased discrepancy in the polarity difference with a fluorinated hydrophobic segment and changes the aggregation state of the polymer in water. The PEG‐fluorinated and trehalose/PEG‐fluorinated amphiphilic random copolymers were the most efficient at encapsulating a fluorinated agrochemical. The small‐molecule agrochemical exerts a strong influence on the self‐assembly of the polymers, demonstrating that fluorous interactions result in not only intramolecular self‐folding behavior but also intermolecular polymer association to form well‐defined nanoparticles. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 352–359     

On-Demand Release of Urea From a Cellulosic Hydrogel Using a Sprinkler Based Irrigation (SBI) Model

In this work, epichlorohydrin (Ech) crosslinked cellulose hydrogels have been prepared and loaded with urea (Ur) for controlled release as a fertilizer. A detailed study of swelling behavior of these hydrogels and their urea releasing capacity has been carried out under various experimental conditions. The dynamic swelling and release data has been applied on various kinetic models. Finally, using a novel Sprinkler Based Irrigation (SBI) model, a model plant has been irrigated with water in the presence of urea-loaded hydrogel. It was found that plants, irrigated in the presence of urea-loaded hydrogel exhibited a better growth as compared to the control plant sample.     

Validating Eaton's Hypothesis: Cubane as a Benzene Bioisostere

Pharmaceutical and agrochemical discovery programs are under considerable pressure to meet increasing global demand and thus require constant innovation. Classical hydrocarbon scaffolds have long assisted in bringing new molecules to the market place, but an obvious omission is that of the Platonic solid cubane. Eaton, however, suggested that this molecule has the potential to act as a benzene bioisostere. Herein, we report the validation of Eaton's hypothesis with cubane derivatives of five molecules that are used clinically or as agrochemicals. Two cubane analogues showed increased bioactivity compared to their benzene counterparts whereas two further analogues displayed equal bioactivity, and the fifth one demonstrated only partial efficacy. Ramifications from this study are best realized by reflecting on the number of bioactive molecules that contain a benzene ring. Substitution with the cubane scaffold where possible could revitalize these systems, and thus expedite much needed lead candidate identification.     

Development and Utilization of a Model System to Evaluate the Potential of Surface Coatings for Protecting Grapes from Volatile Phenols Implicated in Smoke Taint

Due to the increasing frequency of wildfires in recent years, there is a strong need for developing mitigation strategies to manage the impact of smoke exposure of vines and occurrence of ‘smoke taint’ in wine. One plausible approach would be to prevent or inhibit the uptake of volatile phenols from smoke into grape berries in the vineyard. In this study we describe a model system we developed for evaluating under controlled conditions the effectiveness of a range of surface coatings (including existing horticultural sprays) for reducing/preventing the uptake of volatile phenols and their subsequent conversion to phenolic glycosides. Grapes were coated with the materials to be tested and then exposed to gaseous phenols, via evaporation from an aqueous solution, in a semi-closed glass container. Analysis of volatile phenols and their glycosidic grape metabolites demonstrated that the treatments typically did not provide any significant protection; in fact, some resulted in higher concentrations of these compounds in the grapes. The highest concentrations of volatile phenols and their glycosides were observed after application of oily, hydrophobic materials, suggesting that these materials may enhance the adsorption or transfer of volatile phenols into grape berries. Therefore, it is important to consider the types of sprays that are being applied in the vineyard before and during smoke events to prevent the potential of exacerbating the uptake of smoke compounds by grape berries.