排序方式: 共有32条查询结果,搜索用时 0 毫秒
1.
Kira Rubina Edgars AbelePavel Arsenyan Mendel FleisherJuris Popelis Alexander GaukhmanEdmunds Lukevics 《Tetrahedron》2003,59(38):7603-7607
Stereoselective transformations of 2-chlorovinylsulfides in the presence of soluble (t-BuOK) or insoluble (solid KOH or Cs2CO3/18-crown-6) base and palladium catalyst (dppb)Pd(OAc)2 have been studied. Depending on the substrate or catalytic system, the reaction leads to the formation of (E)-1,2-bis[aryl(or arylmethyl)thio]ethenes and/or (E)-1,4-bis[aryl(or arylmethyl)thio]-1-buten-3-ynes in yields of up to 93%. 相似文献
2.
Kira Rubina Edgars Ābele Juris Popelis Solveiga Grinberga Pavel Arsenyan Edmunds Lukevics 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):521-529
A novel two-step method for the preparation of ( E )-2-chlorovinylthioarenes (or hetarenes) from thiols and 1,1,2-trichloroethane in the phase transfer catalytic systems solid K 2 CO 3 /solid KI/18-crown-6/xylene and solid KOH/18-crown-6/toluene has been developed. ( E )-2-chlorovinylthioarenes were isolated in yields up to 98%. Utilization of ( E )-2-chlorovinylthioarenes in the Heck and Stille reactions has been shown. 相似文献
3.
Ene–yne cross metathesis was assessed for use as a key fragment coupling in a planned total synthesis of amphidinolide P. A terminal alkyne containing a β,γ-epoxide was synthesized and employed as the alkyne partner in an intermolecular ene–yne metathesis. In the alkene substrate, optimal functionality and reaction conditions were determined. An unprotected allyl alcohol was found to be critical for both high yield and high E-selectivity. Fewer equivalents of the alkene resulted in incomplete reaction and side reactions consumed the terminal alkyne. The best ruthenium carbene precatalysts were found to be the Hoveyda–Grubbs carbene complexes. 相似文献
4.
Pavel Arsenyan Edgars Paegle Alla Petrenko Sergey Belyakov 《Tetrahedron letters》2010,51(38):5052-5055
A novel, cheap copper(II) fluoride-mediated N-arylation of heterocycles with halothiophenes is described. The yield of the pyrazolylthiophene strongly depends on the nature of the initial thiophene. The molecular structure of 3,5-dimethyl-1-(5′-methyl-[2,2′]bithienyl-5-yl)-1H-pyrazole was studied by X-ray diffraction. 相似文献
5.
A mild, room-temperature Pd-catalyzed acetoxylation of pyrroles with phenyliodonium acetate is described. The acetoxylation was found to proceed via the initial formation of pyrrolyl(phenyl)iodonium acetates, which were converted to acetoxypyrroles in the presence of Pd(OAc)(2). The acetoxylation could also be carried out as a one-pot sequential procedure without the isolation of the intermediate iodonium salts. 相似文献
6.
Peter Spietz Uldis Gross Edgars Smalins Johannes Orphal John P. Burrows 《Spectrochimica Acta Part B: Atomic Spectroscopy》2001,56(12):2465-2478
The 183.038 nm resonance absorption transition of I(2P3/2) has been studied using a flash photolysis set-up for gas-phase chemistry and a radio frequency powered electrodeless discharge lamp filled with iodine. The dependence of self-absorption and self-reversal on iodine partial pressure in the discharge volume was measured. The optimum iodine partial pressure, with self-absorption minimized and acceptable intensity, is determined to be approximately 2.5×10−3 mbar. A method is described to estimate the temperature of the emitting atoms using direct measurements of relative absorption at different absorber concentrations. This yields an emission temperature of 923±50 K. Using this temperature, the oscillator strength for the I(2P3/2) transition at 183.038 nm is determined to be f=(3.87±0.57)×10−3, corresponding to an absorption cross-section at the center of the line of σ=(5.42±0.8)×10−14 cm2 atom−1. This shows a difference from one of two earlier measurements, but is close to the other. The remaining difference from the latter measurement is probably due to tendencies of opposite biases inherent to the experiments. 相似文献
7.
Natural‐Antioxidant‐Inspired Benzo[b]selenophenes: Synthesis,Redox Properties,and Antiproliferative Activity 下载免费PDF全文
Edgars Paegle Dr. Ilona Domracheva Dr. Baiba Turovska Dr. Marina Petrova Dr. Iveta Kanepe‐Lapsa Anita Gulbe Dr. Edvards Liepinsh Dr. Pavel Arsenyan 《化学:亚洲杂志》2016,11(13):1929-1938
The cyclization of arylalkynes under selenobromination conditions, combined with an acid‐induced 3,2‐aryl shift, was elaborated as a general synthetic pathway for the preparation of polyhydroxy‐2‐ and ‐3‐arylbenzo[b]selenophenes from the same starting materials. The redox properties, free‐radical‐scavenging ability, and cytotoxicity against malignant cell lines (MCF‐7, MDA‐MB‐231, HepG2, and 4T1) of the synthesized compounds were explored, and the obtained results were used to consider the structure–activity relationships (SARs) in these compounds. Consequently, the structural features that were responsible for the highly potent peroxyl‐radical‐scavenging activity were established. 相似文献
8.
Sergey Belyakov Edgars Alksnis Velta Muravenko Edmunds Lukevics 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(1):o63-o64
The title compound, C14H11Cl3N4O2, consists of two planar fragments which are nearly perpendicular to one another. The crystal packing is controlled by intra‐ and intermolecular C—H·O hydrogen bonds, and Cl·phenyl‐ring‐centroid and weak stacking interactions. 相似文献
9.
Edgars Abele Ramona Abele Kira Rubina Juris Popelis Ilze Sleiksa Edmunds Lukevics 《合成通讯》2013,43(14):2621-2633
Two simple one-pot phase transfer catalytic methods for the preparation of ketoxime O-ethers from the corresponding ketoximes and alkyl iodides prepared in situ from alkyl chlorides were developed. The corresponding aryl and hetaryl ketoxime O-ethers were obtained in 15–83% yields. 相似文献
10.