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101.
A simple and efficient process has been developed for the synthesis of 1,2,4-oxadiazoles in good yields through the reaction of amidoximes with anhydrides under catalyst-free conditions in water. 相似文献
102.
Li X Tanasova M Vasileiou C Borhan B 《Journal of the American Chemical Society》2008,130(6):1885-1893
A general and sensitive nonempirical protocol to determine the absolute configurations of erythro and threo diols, amino alcohols, and diamines is reported. Binding of diols to the porphyrin tweezer system is greatly enhanced by increasing the Lewis acidity of the metalloporphyrin. Supramolecular complexes formed between the porphyrin tweezer host and chiral substrates exhibited exciton-coupled bisignate CD spectra with predictable signs based on the substituents on the chiral center. The working model suggests that the observed helicity of the porphyrin tweezer is dictated via steric differentiation experienced by the porphyrin ring bound to each chiral center. A variety of erythro and threo substrates were investigated to verify this chiroptical method. Their absolute configurations were unequivocally determined, and thus a general mnemonic is provided for the assignment of chirality. 相似文献
103.
<正>An efficient and mild method for the direct conversion of alcohols into N-alkylphthalimides using 2,4,6-trichloro-1,3,5-triazine and dimethylformamide was described.The reaction was preceded via(alcoxymethylene) dimethylammonium chloride intermediate and produced corresponding N-alkylphthalimides in good-to-excellent yields. 相似文献
104.
105.
Li Cui Ipek Yapici Babak Borhan Gavin E. Reid 《Journal of the American Society for Mass Spectrometry》2014,25(1):141-148
Abundant neutral losses of 98 Da are often observed upon ion trap CID-MS/MS of protonated phosphopeptide ions. Two competing fragmentation pathways are involved in this process, namely, the direct loss of H3PO4 from the phosphorylated residue and the combined losses of HPO3 and H2O from the phosphorylation site and from an additional site within the peptide, respectively. These competing pathways produce product ions with different structures but the same m/z values, potentially limiting the utility of CID-MS3 for phosphorylation site localization. To quantify the relative contributions of these pathways and to determine the conditions under which each pathway predominates, we have examined the ion trap CID-MS/MS fragmentation of a series of regioselective 18O-phosphate ester labeled phosphopeptides prepared using novel solution-phase amino acid synthesis and solid-phase peptide synthesis methodologies. By comparing the intensity of the –100 Da (–H3PO3 18O) versus –98 Da (–[HPO3 + H2O]) neutral loss product ions formed upon MS/MS, quantification of the two pathways was achieved. Factors that affect the extent of formation of the competing neutral losses were investigated, with the combined loss pathway predominantly occurring under conditions of limited proton mobility, and with increased combined losses observed for phosphothreonine compared with phosphoserine-containing peptides. The combined loss pathway was found to be less dominant under ion activation conditions associated with HCD-MS/MS. Finally, the contribution of carboxylic acid functional groups and backbone amide bonds to the water loss in the combined loss fragmentation pathway was determined via methyl esterification and by examination of a phosphopeptide lacking side-chain hydroxyl groups. Figure
? 相似文献
106.
107.
Babak Kaboudin Foad Kazemi Abolfazl Ghaderian Zahra Zand 《Journal of the Iranian Chemical Society》2014,11(4):1121-1127
108.
Sayed Habib Kazemi Babak Karimi Armin Fashi Hesam Behzadnia Hojatollah Vali 《Journal of Solid State Electrochemistry》2014,18(9):2419-2424
This article reports the superior specific capacitance, energy, and power density of a nanofibrillated mesoporous carbon derived from an ionic liquid source (IFMC). It was concluded that high specific capacitance and good electrical conductivity were originated from contribution of nitrogen content of IFMC, also the interesting nanofibrillated structure. A specific capacitance of 235 F g?1 at a high discharge current of 5 A g?1 was estimated for IFMC-based electrode which is higher than the most reported capacitance for carbon materials. An excellent performance of the nanofibrillated mesoporous carbon along with proper concentration of nitrogen constituent in the carbonaceous framework is indicative for important effects of tuning the carbon nanostructure for energy storage applications. 相似文献
109.
Stability and rheological properties of concentrated emulsions (including those for manufacture of vitamin microcapsules) can be related to elementary coalescence acts and adhesion of emulsion drops interacting through thin layers (microscopic emulsion films) of a dispersion medium A new procedure was used for measuring the adhesion force fa between two drops of n-heptane in polymer solutions and lifetime τ of the drops in the contacts depending on the volume concentration C of the polymer, time of formation tf of adsorption layers, temperature T, capillary pressure Pc in the film, surface area S of the film, and on addition of acetone and tannin. The molecular mechanism of the interaction between adsorption layers of polymers and of the process of film destruction is discussed on the basis of the relationships obtained for interaction free energy Δ Fa, activation energy E, destruction activation volume δ and physico-chemical parameters. 相似文献
110.
Ryoko Yasumura Kumar Dilip Ashtekar Akio Tonouchi Tatsuo Nehira Babak Borhan Masaru Hashimoto 《Tetrahedron》2013
Novel 7-β- and 10-β-hydroxylated congeners of CAF-603 (4 and 5, respectively) were isolated from Trichoderma crassum. Relative configuration of 4 was determined by NOE experiments. Stereochemistry of 7-β-hydroxy group in 5 was established by a combination of vicinal 3JH–H analyses and quantum chemical calculations. Absolute configurations of 4 and 5 were established by observing the Cotton effects of their bis(2-naphthoate) esters. T. crassum also produce known CAF-603 (1), 14-hydroxy and 8,9-β-epoxy derivatives (2 and 3, respectively). Present study first established the absolute configuration of CAF-603 family by taking their biosyntheses into account. Preliminary biological experiments revealed that the molecular target strictly recognizes the β-side of the cycloheptane ring. 相似文献