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Bis-dithianylalkanols and dimers are formed in preparation of 2-lithio-1,3-dithianes due to the presence of oxidising impurity in n-BuLi (perhaps n-BuOOLi). 相似文献
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Dhoolesh Gangaram Kokare Krishna Naik Anupama Nevrekar Avinash Kotian Vinayak Kamat Vidyanand K. Revankar 《应用有机金属化学》2016,30(4):181-187
Mononuclear divalent complexes of Co, Ni, Cu and Zn derived from a benzofuran‐based novel hydrazone tridentate ligand were synthesized and characterized using various spectroscopic methods. Elemental analysis reveals that the metal‐to‐ligand ratio is 1:2 which is supported by mass spectrometry results. Conductivity measurements suggest that all the complexes are non‐electrolytic in nature. The ligand and complexes were evaluated for their antimicrobial potency. Bioassay of all hydrazone chelates shows enhanced activity as compared to that of the ligand. The complex with cobalt ion as the metal centre shows better activity against fungi than the standard. Also, ligand and complexes were screened for antituberculosis activity; some analogues (Ni, Cu, Zn) are eight times more active than the standard. Both ligand and complexes show moderate ability to cleave calf thymus DNA. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
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Hu Yuan Kaijian Bi Wanlin Chang Rongcai Yue Bo Li Ji Ye Qingyan Sun Huizi Jin Lei Shan Weidong Zhang 《Tetrahedron》2014
A total synthesis of Daphnodorin A, a member of the Daphnodorins, was accomplished. Key features of the synthetic strategy include construction of 2-substituted-3-functionalized benzofuran via intramolecular Heck reaction and a mild Barton–McCombie deoxygenation process mediated by triethylborane. The total synthesis provided Daphnodorin A in 19.7% or 5.6% overall yield over 7 or 15 steps. 相似文献
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Tiia‐Riikka Tero Dr. Kirsi Salorinne Dr. Heli Lehtivuori Prof. Janne A. Ihalainen Prof. Maija Nissinen 《化学:亚洲杂志》2014,9(7):1860-1867
An unexpected and previously unknown resorcinarene mono‐crown with a fused benzofuran moiety in its macrocyclic core was obtained as a byproduct from a bridging reaction of tetramethoxy resorcinarene with tetraethylene glycol ditosylate. The formation of the fused benzofuran moiety in the resorcinarene macrocycle resulted in a unique rigid and puckered boat conformation, as shown by XRD studies in the solid state. Modification of the macrocycle was also observed to affect the photophysical properties in solution by enhancing the fluorescence brightness compared with a conventional resorcinarene macrocycle. The fluorescent properties enabled unique detection of structural features, that is, the rigid boat conformation with the conjugated benzofuran system and the more flexible crown bridge part, in solution. 相似文献
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Mohammad Shahidul Islam M. Ali Abdullah Mohammed Al-Majid Abdullah Saleh Alamary Saeed Alshahrani Sammer Yousuf Muhammad Iqbal Choudhary Assem Barakat 《Molecules (Basel, Switzerland)》2021,26(8)
The Friedel–Crafts reaction between substituted indoles as nucleophiles with chalcones-based benzofuran and benzothiophene scaffolds was carried out by employing a highly efficient bimetallic iron–palladium catalyst system. This catalytic approach produced the desired bis-heteroaryl products with low catalyst loading, a simple procedure, and with acceptable yield. All synthesized indole scaffolds 3a–3s were initially evaluated for their cytotoxic effect against human fibroblast BJ cell lines and appeared to be non-cytotoxic. All non-cytotoxic compounds 3a–3s were then evaluated for their anticancer activities against cervical cancer HeLa, prostate cancer PC3, and breast cancer MCF-7 cell lines, in comparison to standard drug doxorubicin, with IC50 values 1.9 ± 0.4 µM, 0.9 ± 0.14 µM and 0.79 ± 0.05 µM, respectively, and appeared to be moderate to weak anticancer agents. Fluoro-substituted chalcone moiety-containing compounds, 3b appeared to be the most active member of the series against cervical HeLa (IC50 = 8.2 ± 0.2 µM) and breast MCF-7 cancer cell line (IC50 = 12.3 ± 0.04 µM), whereas 6-fluroindol-4-bromophenyl chalcone-containing compound 3e (IC50 = 7.8 ± 0.4 µM) appeared to be more active against PC3 prostate cancer cell line. 相似文献
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G. Z. Stasevich V. L. Stepanenko M. V. Kudrevatykh O. Yu. Avrutina O. N. Bubel 《Chemistry of Heterocyclic Compounds》2003,39(6):707-712
5-Hydroxy-3-(1-oxo-2,3-epoxyalkyl)benzofurans were obtained with yields of up to 81% by the reaction of p-benzoquinone with oxiranyl -dimethylaminovinyl ketones in acetic acid. 相似文献
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We have developed an effective organometallic‐based procedure allowing the employment of 2‐methylphenols as easily available starting materials in the synthesis of 3‐alkylbenzofuran‐2(3H)‐ones. The first step of this protocol, an anionic homologous Fries‐rearrangement, afforded 2‐(2‐ tert ‐butyldimethylsilyloxyaryl)acetamides, which were selectively metalated and monoalkylated at the benzylic position. Acidic work‐up of crude products afforded the desired heterocycles in satisfactory overall yields. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
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Haichang Zhang Erqian Guo Yujie Fang Peihua Ren Wenjun Yang 《Journal of polymer science. Part A, Polymer chemistry》2009,47(20):5488-5497
The solution processable alternating benzofuran/terfluorene copolymer bearing side oxadiazole groups ( PBF‐OXD ) was synthesized and its optoelectronic properties and color stability were investigated. Electron‐deficient and stereohindered oxadiazole units were used as pendent groups to compensate for the poor electron‐transporting ability of a p‐type polymer backbone, to depress the intermolecular π‐stacking, and to improve solubility while retaining polymer blue emission. PBF‐OXD showed a glass transition at 135 °C and an onset decomposition temperature of ~345 °C. A simple EL device, with the configuration of ITO/PEDOT:PSS/ PBF‐OXD /Ba/Al, displayed a stable blue emission (λmax = 434 nm), good color purity (full width half‐maximum = 59 nm), maximum brightness of 1400 cd/m2, and a maximum luminance efficiency of 0.95 cd/A. The PL and EL spectra changed slightly on annealing and on increasing the applied voltage. These results show that the as‐synthesized copolymer PBF‐OXD had integrated respective functions of its different building blocks and exhibited good thermal and color stability with improved EL performance. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 5488–5497, 2009 相似文献
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《Tetrahedron letters》2003,44(27):4961-4963
o-Formylation of electron-rich phenols is accomplished with dichloromethyl methyl ether and TiCl4. The reaction gives excellent yields, good regioselectivity, and does not leading to diformylation. 相似文献