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81.
Byung Woo Yoo Heung Soo Baek Sam Rok Keum Cheol Min Yoon Ghil Soo Nam Sung Hoon Kim 《合成通讯》2013,43(23):4317-4322
The reductive cleavage of thiobenzoates promoted by samarium diiodide afforded various kinds of disulfides in good yields under mild and neutral conditions. 相似文献
82.
Ok Doo Awh Jae Rok Kim Sung Chul Shim 《Journal of Radioanalytical and Nuclear Chemistry》1988,128(4):299-307
Four stereoisomeric99mTc complexes from meso and racemic 2,3-dimercaptosuccinic acids /DMSA/ were prepared controlling the pH and the molar ratio of ligand to tin/II/ chloride. The complexes showed different thermal stability and lipophilicity. 相似文献
83.
84.
Differential Laser‐Induced Perturbation Spectroscopy for Analysis of Mixtures of the Fluorophores l‐Phenylalanine,l‐Tyrosine and l‐Tryptophan Using a Fluorescence Probe
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Quantitative detection of common endogenous fluorophores is accomplished using differential laser‐induced perturbation spectroscopy (DLIPS) with a 193‐nm UV fluorescence probe and various UV perturbation wavelengths. In this study, DLIPS is explored as an alternative to traditional fluorescence spectroscopy alone, with a goal of exploring natural fluorophores pursuant to biological samples and tissue analysis. To this end, aromatic amino acids, namely, l ‐phenylalanine, l ‐tyrosine and l ‐tryptophan are mixed with differing mass ratios and then classified with various DLIPS schemes. Classification with a traditional fluorescence probe is used as a benchmark. The results show a 20% improvement in classification performance of the DLIPS method over the traditional fluorescence method using partial least squares (PLS) analysis. Additional multivariate analyses are explored, and the relevant photochemistry is elucidated in the context of perturbation wavelengths. We conclude that DLIPS is a promising biosensing approach with potential for in vivo analysis given the current findings with fluorophores relevant to biological tissues. 相似文献
85.
A series of novel N-benzylidenesulfonohydrazide compounds were designed and synthesized as inhibitors of UDP-N-acetylmuramic acid: L-alanine ligase (MurC) and UDP-N-acetylmuramoyl-L-alanine: D-glutamate ligase (MurD) from E. coli, involved in the biosynthesis of bacterial cell-walls. Some compounds possessed inhibitory activity against both enzymes with IC(50) values as low as 30 microM. In addition, a new, one-pot synthesis of amidobenzaldehydes is reported. 相似文献
86.
Edison Thomas Nesakumar Jebakumar Immanuel Sethuraman Mathur Gopalakrishnan Lee Yong Rok 《Research on Chemical Intermediates》2016,42(2):713-724
Research on Chemical Intermediates - This study deals with reduction of ortho and para-nitroaniline by NaBH4 with silver nanoparticles (AgNPs), synthesized by use of a green method, as catalyst. In... 相似文献
87.
Back Cover: Covalent Self‐Assembly and One‐Step Photocrosslinking of Tyrosine‐Rich Oligopeptides to Form Diverse Nanostructures (Angew. Chem. Int. Ed. 24/2016)
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88.
Lee SJ Lee JR Kim YH Park YS Park SI Park HS Kim KP 《Rapid communications in mass spectrometry : RCM》2007,21(17):2797-2804
Protein tyrosine nitration is one of the important regulatory mechanisms in various cellular phenomena such as cell adhesion, endo/exo-cytosis of cellular materials, and signal transduction. In the present study, electrospray ionization tandem mass spectrometry (ESI-MS/MS) with a linear ion-trap mass spectrometer was applied for identification of nitrated proteins and localization of the modified tyrosine residues. When angiotensin II(DRVYIHPF) was nitrated in vitro with tetranitromethane (TNM), the mass spectrum showed a shift of +45 Da which corresponded to tyrosine nitration. An additional +29 Da mass shift was also detected by ESI-MS. This differed from nitrated peptide analysis with matrix-associated laser desorption/ionization mass spectrometry (MALDI-MS), which showed oxygen neutral loss from the nitrated tyrosine residues upon laser irradiation. Hence the +29 Da mass shift of the nitrated peptide observed by ESI-MS suggested the introduction of an NO group for nitrosylation of tyrosine residues. To confirm this in vitro nitrosylation on the protein level, bovine serum albumin was in vitro nitrated with TNM and analyzed by ESI-MS/MS. As expected, +29 as well as +45 Da mass shifts were detected, and the +29 Da mass shift was found to correspond to the modification on tyrosine residues by NO. Although the chemical mechanism by which this occurs in ESI-MS is not clear, the +29 Da mass shift could be a new potential marker of nitrosylated peptides. 相似文献
89.
Pd(0)-catalyzed carbonylation of (Z)-2-en-4-yn carbonates in the presence of a balloon pressure of CO in an alcohol donates vinylallenyl esters with an exclusively E-configuration and in high yields. The fact that no such reactivity could be observed with E-configured enyne carbonates may indicate that the reaction is promoted via the cooperative coordination of palladium with both alkynyl and carbonate moieties. 相似文献
90.
Monika Janjić Rok Prebil Uroš Grošelj David Kralj Črt Malavašič Amalija Golobič Katarina Stare Georg Dahmann Branko Stanovnik Jurij Svete 《Helvetica chimica acta》2011,94(9):1703-1717
A four‐step synthesis of 1‐substituted 5‐(2‐aminophenyl)‐1H‐pyrazoles 5 as a novel type of histamine analogs and versatile building blocks for further transformations was developed. The synthesis starts from commercially available 2‐nitroacetophenone ( 12 ), which is converted into the enamino ketone 13 as the key intermediate. Cyclization of the key intermediate 13 with monosubstituted hydrazines 14a – 14l afforded the 5‐(2‐nitrophenyl)‐1H‐pyrazoles 17a – 17l . Finally, catalytic hydrogenation of the nitro compounds 17a, 17c – 17e , and 17g – 17j furnished the title compounds 5a, 5c – 5e , and 5g – 5j , respectively, in good yields. As demonstrated by some further transformations, additional functionalization of compounds 17 and 5 is feasible, either by electrophilic substitution at C(4) of the pyrazole ring, or at the NH2 group. 相似文献