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981.
N-Arylation of imidazoles with arylboronic acids was efficiently carried out in the presence of a catalytic amount of SiO2-NHC-CuI in methanol at room temperature under base-free reaction conditions. The reactions of a variety of arylboronic acids with imidazoles generated the corresponding products N-arylimidazoles in good to excellent yields. In addition, SiO2-NHC-CuI could be recovered and recycled for six consecutive trials without significant loss of its reactivity. 相似文献
982.
To develop novel oligothiophene‐based liquid crystals involving hydrogen bonding, new terthiophene derivatives containing a stearylamide group, N,N′‐distearyl‐5,5″‐dicyano‐2,2′∶5′,2″‐terthiophene‐4,4″‐dicarboxamide (DNC18DCN 3T) and N,N′‐distearyl‐5,5′‐dipropyl‐2,2′∶5′,2′‐terthiophene‐4,4″‐dicarboxamide (DNC18 DP3T), were designed and synthesized, and their thermal behavior examined. Although DNC18DP3T did not exhibit liquid crystallinity, DNC18DCN3T was found to form smectic A phase. 相似文献
983.
A variety of 2-(1-arylcarbonyl-1-arylazomethylidene)-thiazolidenes were synthesized in excellent yields by the reaction of 2-(arylcarbonylmethylidene)thiazolidines with diazobenzenes. 相似文献
984.
A series of cholesterylated thiogalactosides L1 –L6 the cell targeting ligands for gene delivery to hepatocytes, was synthesized. Related poly(ethylene glycol) chain was used as a bridge for the attachment of galactoside on one hydroxyl end, while the other hydroxyl end was linked with cholesterol. This design provided an effective entry for the synthesis of a poly(ethylene glycol) compound with the hepatocyte targeting. 相似文献
985.
In the presence of 1,8-diazabicycolo[5.4.0]undec-7-ene (DBU) and concentrated H2SO4, 2-naphthol reacted smoothly with α,β-unsaturated trifluoromethyl ketones in CH2Cl2 at room temperature, affording the 3-trifluoromethyl-substituted benzo[f]chromene derivatives in good to excellent yields in a one-pot reaction. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource: Full experimental and spectral details]. 相似文献
986.
A convenient and sustainable synthesis of pyrazolo[1,5-a]quinazolin-5(4H)-ones and [1,2,4]triazolo[1,5-a]quinazolin-5(4H)-one through copper-catalyzed cascade reactions of 2-bromobenzoates with 1H-pyrazol-5-amines or 1H-1,2,4-triazol-5-amine under ligand-free conditions in water is presented. It is notable that aqueous medium turned out to be crucial for the chemoselective formation of the title compounds. Compared with literature protocols, this new method showed advantages such as simple and sustainable procedure, commercially available starting materials, and convenient reuse of the reaction medium together with the copper catalyst. 相似文献
987.
The C1–8 fragment of autolytimycin was synthesized via a reliable 10-step route capable of delivering 41% overall yield at multi-gram scale. As a key step, a chelation-controlled isopropenylation of α-oxygenated aldehydes was established with a reagent combination of diisopropenylzinc, magnesium halide, and a dichloromethane/toluene mixed solvent. Cram-chelate isopropenylation products dominated for aldehydes with a small α-substituents, such as –OMe and –OBn groups, while the Felkin product could be obtained with a bulky –OTBS group. 相似文献
988.
AbstractA convenient and efficient procedure for the synthesis of 2-substituted-6,7-dihydrobenzo[d]oxazol-4(5H)-ones and 2-aryl-6,7-dihydrobenzofuran-4(5H)-ones through a Rh2(OAc)4-catalyzed C≡X (X?=?N, C) insertion of cyclic 2-diazo-1,3-diketones with nitriles and aromatic alkynes has been developed. This reaction uses readily available starting materials and stable cyclic 2-diazo-1,3-diketone compounds, with desired products formed in good to high yields. A tentative mechanism involving a C≡X bond insertion and 1,5-dipolar electrocyclization/ring opening and cyclization sequence for this reaction is proposed. 相似文献
989.
Mingming Zou Ying Li Jun Wang Qi Wang Yumei Kong Jingqun Gao Ping Fan 《Journal of solution chemistry》2013,42(4):849-865
The interaction between bovine serum albumin (BSA) and FeIII complexes with three binary organic acid (biorga) ligands, [FeIII(oxa)(H2O)4]+ (oxa = oxalic acid), [FeIII(pra)(H2O)4]+ (pra = propanedioic acid) and [FeIII(sua)(H2O)4]+ (sua = succinic acid), as well as the sonocatalytic damage of BSA in the presence of these three FeIII–biorga complexes under ultrasonic irradiation, were studied by UV–vis and fluorescence spectra. The experimental results show that the fluorescence quenching process of BSA caused by three FeIII–biorga complexes are all static quenching and the corresponding quenching rate constants (K q), equilibrium constants (K A) and the binding site numbers (n) were calculated. The results reveal that, under ultrasonic irradiation, the BSA molecules were obviously damaged by these FeIII–biorga complexes. In addition, the effects of several factors on the damage of BSA molecules were examined. The experimental results demonstrate that the damage degree of BSA increased with an increase of ultrasonic irradiation time, FeIII–biorga complex concentration, and ionic strength. In comparison, [FeIII(pra)(H2O)4]+ exhibited higher sonocatalytic activity than [FeIII(oxa)(H2O)4]+ and [FeIII(sua)(H2O)4]+. Finally, the extent of generation of $ \cdot {\text{O}}_{2}^{ - } $ · O 2 ? and ·OH during sonocatalytic processes was estimated. Perhaps, the results will be significant for promoting sonodynamic treatment (SDT) of tumors at the molecular level. 相似文献
990.
Nadezhda I. Islamova Xi ChenChang-Jun Fan Richard S. AndinoWatson J. Lees 《Polymer Degradation and Stability》2013
Photochromic indolylfulgimides covalently attached to polymers have beneficial properties for optical switching. A 3-indolylfulgide and two 3-indolylfulgimides with one or two polymerizable styrene groups attached on the nitrogen atom(s) were synthesized. Copolymerization with methyl methacrylate (MMA) provided linear copolymers (one styrene group) or a cross-linked copolymer (two styrene groups). The properties of the monomers and copolymers in toluene or as thin films were characterized. The new copolymers were photochromic (reversible Z-to-C isomerization), absorbed visible light, and revealed good thermal and photochemical stability. At room temperature, all copolymer films showed no loss of absorbance after 5 weeks. At 80 °C in either toluene or as films, the Z-forms copolymers were less stable than the C-form copolymers, which showed little or no degradation after 400 h. The degradation rate due to repeated ring-closing – ring opening cycles was less than 3% per 100 cycles. The cross-linked copolymer showed photochemical stability comparable to monomeric fulgides in toluene, <1% per 100 cycles. In general, the properties of the linear and cross-linked copolymers were similar to the corresponding monomers in toluene. In films, the conformations of the Z-form were restricted due to the matrix indicating that the preparation of films from the C-form is advantageous. 相似文献