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11.
Kui Wu Nathan A. Yee Sangeetha Srinivasan Amir Mahmoodi Michael Zakharian Jose M. Mejia Oneto Maksim Royzen 《Chemical science》2021,12(21):7583
Correction for ‘Click activated protodrugs against cancer increase the therapeutic potential of chemotherapy through local capture and activation’ by Kui Wu et al., Chem. Sci., 2021, 12, 1259–1271, DOI: 10.1039/D0SC06099B.The authors regret that the reference to the bond-breaking bioorthogonal chemistry, termed ‘click-to-release’ was omitted from the original article. In addition, we would like to include a reference describing the synthesis of compound 1, which is an intermediate to the protodrugs described in the original article. These references are listed below as ref. 1 and 2.The Royal Society of Chemistry apologizes for these errors and any consequent inconvenience to authors and readers. 相似文献
12.
Mir Ali Farajzadeh Mortaza Ebrahimi Ali Ranji Elham Feyz Vali Bejani Amir Abbas Matin 《Mikrochimica acta》2006,153(1-2):73-78
High performance liquid chromatography (HPLC) and gas chromatography (GC) are introduced for analysis of polymer lubricants
(stearamide, oleamide and erucamide). In the HPLC method, a reverse phase octadecylsilane (ODS) column along with acetonitrile/methanol
(60:40) as a mobile phase were used. Detection of analytes was performed by a UV detector at 202 nm. The analysis time was
less than 8 min. In the GC method, polar capillary column and flame ionization detector (FID) were used for separations and
detection, respectively. The analysis time by GC was longer than HPLC and was about 30 min. Limits of detection, linear range
and repeatability of both methods are similar, but determination of oleamide in real samples by HPLC method is difficult due
to complexity of the initial part of HPLC chromatogram in polyethylene samples. That problem is not observed in the GC method.
Detection limits in both methods for all analytes are lower than 0.003% which are much lower than the amount of lubricants
in commercial polymers (0.05–0.2%). 相似文献
13.
Journal of Optimization Theory and Applications - Coordinate descent algorithms are popular in machine learning and large-scale data analysis problems due to their low computational cost iterative... 相似文献
14.
Alan R. Katritzky Amir S. Afridi Wojciech Kuzmierkiewicz 《Helvetica chimica acta》1991,74(8):1931-1935
tert-Alkyl sulfides, with an α-(1H-benzotriazol-1-yl) group 6 and 13 , are readily prepared from N-[(aryl-thio)methyl]-1H-benzotriazoles 3 and N-( 11 ), respectively, by reaction with BuLi and then with the appropriate electrophile. The tert-alkyl sulfides 6 and 13 are smoothly converted by BF3. OEt2 into vinyl sulfides 5, 7 or 12 , respectively, in satisfactory yields. 相似文献
15.
The first examples of intramolecular Zr-catalyzed electrophilic alkylation of aryl olefins are disclosed. Substituted carbo- and heterocycles are prepared efficiently and diastereoselectively. 相似文献
16.
Amir Al-HaddadHessa Al-Kendari 《European Polymer Journal》2002,38(2):265-272
The kinetics of liquid crystalline copolyester synthesis via melt transesterification between poly(butylene terephthalate) (PBT), terephthalic acid (TA) and hydroquinone diacetate (HQDA) is examined. Two different copolyester compositions PBT30/(HQDA+TA) 70 and PBT 50/(HQDA+TA) 50 mol% ratio were synthesized. The ratio of HQDA to TA was kept constant for all the reactions.The copolyesters were synthesized via melt polycondensation route at 265°C, 275°C and 285°C using two different transesterification catalysts, zinc acetate and dibutyl tin oxide. A key postulation assumed in this work is that the reaction originates between TA and HQDA to form a dimer which slices PBT chain. The copolyesterification rate constant for a system containing butylene glycol a more nonpolar moiety compared to ethylene glycol in poly(ethylene terephthalate) has been determined. The activation energy values for the different copolymer systems has also been determined. The rate constants for the uncatalyzed and catalyzed copolyesterification reaction and the activation energy values for the reaction have been determined. 相似文献
17.
New mixed-ligand copper(I) complexes, [Cu(Phca2en)(PPh3)X], [Phca2en = N,N′-bis(β-phenylci-nnamaldehyde)-1,2-diiminoethane and X=Cl (1), Br (2), I (3), NCS (4), N3 (5)] have been synthesized and characterized by various techniques. 1H and 13C-NMR and IR spectral data of these copper(I) complexes are compared with the free ligand to elucidate some structural features. The structures of [Cu(Phca2en)(PPh3)Br] (2) and [Cu(Phca2en)(PPh3)I] (3) have been determined from single-crystal data showing that the coordination geometry around copper atom is a distorted tetrahedron. Furthermore, these Cu(I) complexes exhibit supramolecular motifs of the type multiple phenyl embraces resulting from attractive interactions between phenyl rings of PPh3 moieties. The presence of the C–H…Cu weak intramolecular hydrogen bonds, due to the trapping of C–H bonds in the vicinity of the metal atoms, is also reported. 相似文献
18.
A novel membrane sensor for selective monitoring of iodide, consisting of a triiodide‐ketoconazole ion pair complex dispersed in a PVC matrix, plasticized with a mixture of 2‐nitrophenyl octyl ether and dioctylphtalate with unique selectivity toward iodide ions, is described. The influence of membrane composition, pH of test solution and foreign ions on the electrode performance were investigated. The optimized membrane demonstrates a near‐Nernstian response for iodide ions over a wide linear range from 1.0 × 10?2 to 1.0 × 10?5 M, at 25 ± 1 °C. The electrode could be used over a wide pH range 3–10 and has the advantages of high selectivity, fast response time and good lifetime (over 4 months). It was successfully used as indicator electrode in potentiometric titrations and direct potentiometric assay of iodide ions. 相似文献
19.
A simple colorimetric method for the assay of penicillin G salt and penicillamine by oxidation with iodate 总被引:1,自引:0,他引:1
A simple colorimetric procedure is described for determination of penicillin G salt and penicillamine. It is based on oxidation with potassium iodate at room temperature and measurement of the liberated iodine at 520 nm after extraction with carbon tetrachloride. Compared with other procedures, this method proved to be more rapid, highly reproducible and reasonably accurate. The relative standard deviation did not exceed 0.9% and 0.4% for penicillin and penicillamine, respectively. The procedure has been successfully applied to pharmaceutical preparations containing either of the two compounds. 相似文献
20.
Abid Hussain Heng-Chao Li Muqadar Ali Samad Wali Mehboob Hussain Amir Rehman 《Entropy (Basel, Switzerland)》2022,24(10)
In recent years, searching and retrieving relevant images from large databases has become an emerging challenge for the researcher. Hashing methods that mapped raw data into a short binary code have attracted increasing attention from the researcher. Most existing hashing approaches map samples to a binary vector via a single linear projection, which restricts the flexibility of those methods and leads to optimization problems. We introduce a CNN-based hashing method that uses multiple nonlinear projections to produce additional short-bit binary code to tackle this issue. Further, an end-to-end hashing system is accomplished using a convolutional neural network. Also, we design a loss function that aims to maintain the similarity between images and minimize the quantization error by providing a uniform distribution of the hash bits to illustrate the proposed technique’s effectiveness and significance. Extensive experiments conducted on various datasets demonstrate the superiority of the proposed method in comparison with state-of-the-art deep hashing methods. 相似文献