Hydrazine-hydroquinone complex as an efficient solid phase hydrazine donor: high yield synthesis of luminol and isoluminol

2011 ◽  
Vol 35 (6) ◽  
pp. 326-328 ◽  
Author(s):  
Gautam Chattopadhyay ◽  
Partha Sinha Ray
Keyword(s):  
2019 ◽  
Vol 16 (7) ◽  
pp. 1024-1031
Author(s):  
Diparjun Das ◽  
Kalyani Rajkumari ◽  
Lalthazuala Rokhum

Aim and Objective: Sustainable production of fine chemicals both in industries and pharmaceuticals heavily depends on the application of solid-phase synthesis route coupled with microwave technologies due to their environmentally benign nature. In this report, a microwave-assisted esterification reaction using polymer-bound triphenylphosphine and 4,4′-dinitroazobenzene reagent system was investigated. Materials and Methods: The solvents were obtained from Merck India. Polymer-bound triphenylphosphine (~3 mmol triphenylphosphine moiety/g) was acquired from Sigma-Aldrich. The progress of the reaction was observed by thin-layer chromatography. All the reactions were performed in Milestones StartSYNTH microwave. The NMR spectra were recorded on Bruker Avance III 300, 400, and 500 MHz FT NMR Spectrometers. Using azo compound and polymer-bound triphenyl phosphine as a coupling reagent, esterification of different carboxylic acids with alcohols was performed under microwave irradiation. Results: Esterification of benzoic acid with 1-propanol under microwave irradiation gave a high yield of 92% propyl benzoate in 60 minutes only. Isolation of the ester products was relatively simple as both the byproducts polymer-bound triphenylphosphine oxide and hydrazine could be removed by simple filtration. The rates of reactions were found to be directly proportional to the pKa of the benzoic acids. Conclusion: 4,4′-Dinitroazobenzene was introduced as a novel coupling reagent, in conjugation with polymer-bound triphenylphosphine, for esterification reactions under microwave irradiation. The low moisture sensitivity of the reaction system, easy separation of the byproducts, and column chromatographyfree isolation of esters help our methods with application significance, particularly from the ‘Sustainable Chemistry’ perspective.


2020 ◽  
pp. 415-423
Author(s):  
Elena Vladimirovna Isaeva ◽  
Ol'ga Olegovna Mamaeva ◽  
Tat'yana Vasil'yevna Ryazanova

The purpose of this work was to assess the suitability of solid and liquid waste generated during processing of the vegetative part of poplar as substrates for biochemical processing in order to obtain biologics for various purposes. For the study, we used post-extraction residues, as well as a cubic liquid formed after distilling essential oils and extracting alcohol-soluble substances from the vegetative part of the balsamic poplar (Populus balzamifera L.). Siberian strains of fungi of the genus Trichoderma used as a biodestructor. Studies have shown that the vegetative part of poplar and its individual elements are an available substrate for the growth of mycelial fungi. The high yield of spores (4.5×109 spor/g) and the formation of humic substances (11%) used as plant growth stimulators during solid-phase cultivation of the MG-97 strain of Trichoderma fungi gives grounds to use the vegetative part of poplar as a technological raw material for obtaining a biological product of the "Trichodermin" type or soil humification. Depending on the purpose of the preparations, the duration of cultivation can vary: for obtaining agricultural biologics up to 15 days, more – for soil humification. The inclusion of a cubic liquid at the stage of substrate humidification allows to obtain a biological product with a higher spore titer (5×109 spor/g), makes it possible to close the water consumption cycle and make the technology of processing the vegetative part of poplar waste-free.


2014 ◽  
Vol 21 (12) ◽  
pp. 1257-1264
Author(s):  
Stevenson Flemer

A proof-of-principle methodology is presented in which all commercially-available cysteine (Cys) and selenocysteine (Sec) solid phase peptide synthesis (SPPS) derivatives are synthesized in high yield from easily prepared protected dichalcogenide precursors. A Zn-mediated biphasic reduction process applied to a series of four bis-Nα-protected dichalcogenide compounds allows facile conversion to their corresponding thiol and selenol intermediates followed by insitu S- or Se-alkylation with various electrophiles to directly access twenty one known Cys and Sec SPPS derivatives. Most of these derivatives were able to be precipitated in crude form out of petroleum ether in sufficient purity for direct use as peptide building blocks. Subsequent incorporation of these derivatives into peptide models nicely illustrates their viability and applicability toward SPPS.


1991 ◽  
Vol 44 (6) ◽  
pp. 771 ◽  
Author(s):  
JW Perich ◽  
RM Valerio ◽  
PF Alewood ◽  
RB Johns

A solid phase method is described for the synthesis of O- phosphoseryl-containing peptides by the use of polystyrene resin (Merrifield) as the peptide support and protected Boc-Ser(PO3R2)-OH derivatives for the incorporation of the phosphorylated seryl residue. The viability of this solid phase approach was demonstrated by the synthesis of HBr.H-Glu-Ser (PO3Et2)-Leu-OH in high yield by the use of Bo -Ser(PO3Et2)-OH in peptide synthesis and subsequent use of HBr/CF3CO2H for cleavage of the Ser(PO3Et2)-containing tripeptide from the resin support. Similarly, the dipeptide, CF3CO2H.H-Ser(P)- Leu -OH, was prepared in high yield by using Boc -Ser(PO3But2)-OH in peptide synthesis followed by the one-step deprotection of the Ser(PO3But2)- dipeptide resin by treatment with HBr/CF3CO2H (90 min). Alternatively, the O-phosphoseryl tripeptide , CF3CO2H.H-Glu-Ser(P)- Leu -OH was prepared by using either Ppoc -Ser(PO3Bzl2)-OH or Boc-Ser(PO3Ph2)-OH in peptide synthesis. The one-step deprotection of the Ser(PO3Bzl2)-containing tripeptide and cleavage of the peptide from the resin support was effected by high-pressure hydrogenolysis (palladium acetate). In the case of phenyl phosphate protection, the Ser(PO3Ph2)-containing peptide was cleaved from the resin support by high-pressure hydrogenolysis (palladium acetate) followed by cleavage of the phenyl phosphate groups by platinum-mediated hydrogenolysis (1.0 equiv. PtO2/phenyl group) in 50% CF3CO2H/AcOH.


2020 ◽  
Author(s):  
Thissa N. Siriwardena ◽  
Bee-Ha Gan ◽  
Thilo Köhler ◽  
Christian van Delden ◽  
Sacha Javor ◽  
...  

<p>Solid-phase peptide synthesis (SPPS) is usually performed with optically pure building blocks to prepare peptides as single enantiomers. Herein we report that SPPS using racemic amino acids provides stereorandomized (<i>sr</i>) peptides, containing up to billions of different stereoisomers,<a> </a>as well-defined single HPLC peak, single mass products with high yield, which can be used to investigate peptide bioactivity. To exemplify our method, we show that stereorandomization abolishes the membrane disruptive effect of α-helical amphiphilic antimicrobial peptides but preserves their antibiofilm effect, implying different mechanisms involving folded versus disordered conformations. For antimicrobial peptide dendrimers by contrast, stereorandomization preserves antibacterial, membrane disruptive and anti-biofilm effects but reduces hemolysis and cytotoxicity, thereby increasing their therapeutic index. Finally, we identify partially stereorandomized analogs of the last resort cyclic peptide antibiotic polymyxin B with preserved antibacterial activity but lacking membrane disruptive and lipopolysaccharide neutralizing activity, pointing to the existence of additional targets.</p>


Author(s):  
Christos Zikos ◽  
Alexandra Evangelou ◽  
Dimitra Benaki ◽  
Emmanuel Mikros ◽  
Maria Pelecanou ◽  
...  

1998 ◽  
Vol 64 (6) ◽  
pp. 2200-2206 ◽  
Author(s):  
Jalal Hawari ◽  
A. Halasz ◽  
L. Paquet ◽  
E. Zhou ◽  
B. Spencer ◽  
...  

The present study describes the biotransformation of 2,4,6-trinitrotoluene (TNT) (220 μM) by using anaerobic sludge (10%, vol/vol) supplemented with molasses (3.3 g/liter). Despite the disappearance of TNT in less than 15 h, roughly 0.1% of TNT was attributed to mineralization (14CO2). A combination of solid-phase microextraction–gas chromatography-mass spectrometry and liquid chromatography-mass spectrometry identified two distinctive cycles in the degradation of TNT. One cycle was responsible for the stepwise reduction of TNT to eventually produce triaminotoluene (TAT) in relatively high yield (160 μM). The other cycle involved TAT and was responsible for the production of azo derivatives, e.g., 2,2′,4,4′-tetraamino-6,6′-azotoluene (2,2′,4,4′-TA-6,6′-azoT) and 2,2′,6,6′-tetraamino-4,4′-azotoluene (2,2′,6,6′-TA-4,4′-azoT) at pH 7.2. These azo compounds were also detected when TAT was treated with the anaerobic sludge but not with an autoclaved sludge, suggesting the biotic nature of their formation. When the anaerobic conditions in the TAT-containing culture medium were removed by aeration and/or acidification (pH 3), the corresponding phenolic compounds, e.g., hydroxy-diaminotoluenes and dihydroxy-aminotoluenes, were observed at room temperature. Trihydroxytoluene was detected only after heating TAT in water at 100°C. When 13CH3-labeled TNT was used as the N source in the above microcosms, we were unable to detect13C-labeled p-cresol or [13CH3]toluene, indicating the absence of denitration or deamination in the biodegradation process. The formation and disappearance of TAT were not accompanied by mineralization, suggesting that TAT acted as a dead-end metabolite.


Author(s):  
Calvin F. Miller ◽  
E. Bruce Watson ◽  
T. Mark Harrison

ABSTRACTThe pursuit of a comprehensive theory for the origin and evolution of granitoids is hindered by our incomplete understanding of the nature of the source and the mechanisms by which the magma is segregated and transported. This paper is a collection of three largely independent and necessarily incomplete perspectives on these outstanding issues. Lower to mid-crustal regions, which contain the principal source material for granitoid magmas, are highly heterogeneous. Consideration of available transfer mechanisms suggests that (1) this heterogeneity survives all foreseeable lower crustal processes; (2) closure is on very different scales for different chemical systems (e.g. Pb, Nd, Sr and O isotopes); in almost all cases, however, closure scale is much smaller than the scale of magma extraction zones for plutons; and (3) pluton-wide homogenisation of magmas by diffusion is precluded by low diffusivities in felsic melts. Thus, granitoid magmas begin life as aggregates of small, isolated chemical domains; homogenisation occurs only through (and on the scale of) effective stirring by convection. Because of variability in local conditions as well as in bulk composition, crustal regions undergoing anatexis must be patchworks with variable melt fractions and melt compositions. The way in which magma is extracted from and coalesces with this patchwork exerts a critical influence on the nature of granitoid magmas. Decoupling and unusual coupling of compositional parameters and isotopic heterogeneity within plutons are to be expected in crust-derived granitoids and do not require contamination. Granites image their sources, but these sources are ill-defined and do not correspond to simple, easily-recognised materials. Extent and patterns of heterogeneity remaining in crystallised plutons may be effective indicators of the ascent process.The efforts of materials scientists in characterising the nature and evolution of solid-phase interconnectivity in partially-molten materials may offer some insights into crustal magmatic processes. In particular, the rheological properties of partially-molten crustal rocks are probably strongly affected by the contiguity of the solid grains in the system (i.e. the fraction of their surface area that is shared with other grains). Theory and experimental data for simple alloy systems reveal that contiguity depends principally upon melt fraction and upon the characteristic wetting angle (θ) of the system. Measured θ's in granitoids (∼50° on average) imply contiguities as high as ∼0·2 for melt fractions of 0·5 or greater. This value in turn suggests that, at least under static conditions, a continuous skeleton of solid grains is maintained to quite high degrees of melting in the crust. Consequently, regions consisting of 50% or more of melt can, in principle, maintain not only high yield strength, but also high viscosity (provided the strain rate is sufficiently low to avoid disrupting contiguity).Despite the fact that on some time scale the continuous solid skeleton of a partially-molten region resists deformation, it is itself subject to textural evolution that could lead to the upward migration of melt. Occasional detachment of grains from the skeleton and subsequent “microsettling” within the partially-molten column may lead eventually to compaction of the solid (without plastic deformation) and net upward displacement of melt.Proposed granite transport mechanisms are discussed, although several are viewed as having historical interest only. In the absence of tectonic transport, diapirism appears to be the most compelling of these processes. However, considerable diversity exists in the literature regarding a pivotal requirement for this mechanism. Structural studies have tended to conclude that the granite diapir must be highly crystallised in order to ascend, whereas results of physical modelling yield contradictory results. For ascent to occur in these models, the magmas must be sufficiently fluid to allow convective circulation. Indeed, heat loss associated with diapirism is so efficient as to be a significant restriction on overall ascent. The resolution of these contrasting views appears to be that they reflect different phases of the ascent/emplacement continuum. Understanding the emplacement history of a southeastern Australian pluton allows assessment, via the diapir model, of the flow properties of the rock within the deformation aureole. Results suggest rock viscosities about an order of magnitude lower than those predicted by laboratory experiments, perhaps reflecting difficulties in reproducing natural conditions in the laboratory.


2021 ◽  
Vol 8 ◽  
Author(s):  
Yuyin Dai ◽  
Ri Sa ◽  
Feng Guan ◽  
Qi Wang ◽  
Yinghua Li ◽  
...  

Background: To optimize [18F] 9-fluoropropyl-(+)-dihydrotetrabenazine (18F-FP-(+)-DTBZ) purification via solid-phase extraction (SPE) with combined cartridges to facilitate its widespread clinical application.Methods: A modified SPE purification method, employing Sep-Pak PS-2 and Sep-Pak C18 cartridges, was used for the preparation of 18F-FP-(+)-DTBZ. This method was compared to the purification method of high-pressure liquid chromatography (HPLC) and SPE with one cartridge, following quality control test and positron emission tomography (PET) imaging in healthy volunteers and patients with parkinsn's disease (PD).Results: A SPE purification method integrating Sep-Pak PS-2 and Sep-Pak C18 cartridges was implemented successfully. The retention time of 18F-FP-(+)-DTBZ purified by HPLC, SPE with Sep-Pak PS-2, SPE with Sep-Pak C18, and SPE with combined use of Sep-Pak PS-2 and Sep-Pak C18 cartridges was 8.7, 8.8, 8.7, and 8.9 min, respectively. Fewest impurity peak was detected in 18F-FP-(+)-DTBZ purified by the SPE with combined use of Sep-Pak PS-2 and Sep-Pak C18 cartridges. This modified SPE purification method provided a satisfactory radiochemical yield of 29 ± 1.8% with radiochemical purity &gt;99% and shortened synthesis time to 27 min. The brain uptake of 18F-FP-(+)-DTBZ purified by the modified SPE was comparable to that purified by HPLC in both healthy volunteers and PD patients.Conclusions: A SPE method integrating Sep-Pak PS-2 and Sep-Pak C18 cartridges for purification of 18F-FP-(+)-DTBZ may be highly suited to automatic synthesis for routine clinical applications, as it provides excellent radiochemical purity, high yield as well as operational simplicity.


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