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排序方式: 共有159条查询结果,搜索用时 15 毫秒
1.
2.
The 3',5'-bis-O-TBDMS derivative of 2'-deoxyguanosine can be converted to its O6-alkyl and O6-aryl ethers as well as to N6-substituted diaminopurine nucleosides in two simple steps. Also described is a novel, nonaqueous, one-step O6-desulfonylation method that leads to deprotection of the carbonyl moiety of 2'-deoxyguanosine. 相似文献
3.
Lakshman MK Ngassa FN Bae S Buchanan DG Hahn HG Mah H 《The Journal of organic chemistry》2003,68(15):6020-6030
Single-electron oxidation of the carcinogenic hydrocarbon benzo[a]pyrene (BaP) is thought to result in a radical cation intermediate and this species has been proposed to cause alkylation at the nitrogens of the purine nucleobases. Although several different nucleoside adducts have been isolated as arising from this mode of metabolic activation, there are no selective, total syntheses of the stable exocyclic amino group adducts formed by the single-electron oxidation of any hydrocarbon with the purine 2'-deoxynucleosides to date. In this paper we disclose the synthesis of the model adducts N(6)-(1-pyrenyl)-2'-deoxyadenosine and N(2)-(1-pyrenyl)-2'-deoxyguanosine as well as the first synthesis of the carcinogen-linked nucleoside derivatives N(6)-(6-benzo[a]pyrenyl)-2'-deoxyadenosine and N(2)-(6-benzo[a]pyrenyl)-2'-deoxyguanosine via a palladium-mediated C-N bond formation. Two different coupling strategies were attempted: coupling of an aryl bromide with a suitably protected nucleoside and the coupling of an arylamine with a suitable halonucleoside. The former had somewhat limited applicability in that only N(6)-(1-pyrenyl)-2'-deoxyadenosine was prepared by this method; on the other hand, the latter was more general. However, there are noteworthy differences in the amination reactions at the C-6 and C-2 positions. Reactions at the C-6 resulted in the competing formation of a 1:2 amine-nucleoside adduct in addition to the desired monoaryl nucleoside. Such a dimer formation was not observed at the C-2. The C-2 adducts, however, displayed an interesting conformational behavior. 相似文献
4.
Pd-catalyzed coupling of the axially constrained, less reactive benzo[a]pyrene bay-region amino benzoates, derived from the tetrahydro and diol epoxides, with C-6 and C-2 halopurine deoxynucleosides offers an efficient approach to the synthesis of the corresponding nucleoside-epoxide adducts. Also reported are the first examples involving the coupling of a 6-chloropurine deoxynucleoside with these amines, a reaction that is difficult by direct halide displacement. Certain mechanistic aspects of this metal-catalyzed C-N bond formation are also discussed. [reaction--see text] 相似文献
5.
The electronic absorption spectrum of the Fe2+ ion doped in ammonium chloride has been studied at room and liquid air temperatures. The observed bands have been assigned transitions from the ground 6A1g(S) state to the excited 4A1g(4Eg), 4T1g(G) and 4T2g(G) states. The cubic field approximation with Dq = 675 cm?1, B = 645 cm?1 and C = 4.4 B is found to give a good fit to the observed band positions.It is further concluded that the site symmetry of the Fe3+ ion in the crystal is lowered from Oh to C4v symmetry at liquid air temperature. 相似文献
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Taniya M. S. K. Pathiranage Dushanthi S. Dissanayake Crystal N. Niermann Yixin Ren Michael C. Biewer Mihaela C. Stefan 《Journal of polymer science. Part A, Polymer chemistry》2017,55(20):3327-3346
Semiconducting polythiophenes display electroactive properties which make them excellent candidates for applications as electroactive materials. Ability to undergo doping and to switch between different oxidation states allow tuning the chemical and physical properties of polythiophenes. Furthermore, the ability to integrate polythiophenes into copolymers, hybrid composites with metals and inorganic materials make them useful in electronic and biomedical applications. The capability to vary the properties of the final material with low production cost and high processability into thin films makes polythiophenes desirable materials for many applications. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 3327–3346 相似文献
9.
Kumari J. M. K. W. Senadeera G. K. R. Weerasinghe A. M. J. S. Thotawatthage C. A. Dissanayake M. A. K. L. 《Journal of Solid State Electrochemistry》2021,25(2):695-705
Journal of Solid State Electrochemistry - Ionically conducting gel polymer electrolytes can be used effectively to improve the problems associated with liquid electrolytes in dye-sensitized solar... 相似文献
10.
Gold Decorated Graphene by Laser Ablation for Efficient Electrocatalytic Oxidation of Methanol and Ethanol
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V. Lakshman Kumar R. S. Sai Siddhardha Adarsh Kaniyoor Ramakrishna Podila Muralikrishna Molli Sai Muthu Kumar V K. Venkataramaniah S. Ramaprabhu A. M. Rao Sai Sathish Ramamurthy 《Electroanalysis》2014,26(8):1850-1857
A well‐known limitation in the fabrication of metal‐graphene composite has been the use of surfactants that strongly adsorb on the surface and reduce the performance of the catalyst. We demonstrate here a novel one‐pot synthesis of gold nanoparticles by laser ablation of gold strip and in‐situ decoration on graphene substrate. Not only the impregnation of nanoparticles was linker free, but also the synthesis by itself was surfactant‐free. The composite materials were well characterized morphologically and functionally using electron microscopy, X‐ray and electron diffraction, Raman spectroscopy, Zeta potential, electrochemical measurements and UV‐Visible spectroscopic techniques. This linker‐free gold‐graphene based composite has been employed for catalytic applications pertaining to electrooxidation. We have explored the use of this composite as a binder‐free electrode in electrocatalytic oxidation of methanol and ethanol in alkaline medium. Additionally, the onset potential for ethanol oxidation was found to be more negative, ?100 mV, an indication of its promising application in direct ethanol fuel cells. 相似文献