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Acetylene-azide click macrocyclization of peptides- and 1, 5-disubstituted 1, 2, 3-triazoles. Special attention is given to the Ugi/click strategy

Thiacalix[4]arene-functionalized vesicles as phosphorescent indicators for pyridoxine detection in aqueous solution-tert-butylthiacalix[4]arene were obtained by click reactions of the corresponding azido derivatives with acetylene

Synthesis of Triazolylisatins Glycoconjugates and Some Ammonium Hydrazones on Their BasisAbstract: The click reaction of propargylisatins with some azido-sugars was used to synthesize new

AZT 5'-phosphonates: Achievements and trends in the treatment and prevention of HIV infectionDespite the numerous drawbacks, 3'-azido-3'-deoxythymidine (AZT, Zidovudine, Retrovir) remains one

The ability of choline derivatives synthesized by multi-component reactions in the inhibition of ache enzyme and the molecular diversity, which are highly step-economical reactions. The Ugi reaction, one of the most common

Carbon Stocks and Fluxes in Soils of the Urban Park in Grozny CityDevelopment of urban green infrastructures (UGI) is considered among the main nature

Synthesis, structure, and characterization of high-energy 4,6-diazido-n-(4,6-diazido-1,3,5-triazin-2-yl)-1,3,5-triazin-2-amine did not undergo azido-tetrazole tautomerism in DMSO solutions and existed solely in the azide form

The "click-on-tube" approach for the production of efficient drug carriers based on oxidized multi-walled carbon nanotubes© 2016 The Royal Society of Chemistry.To demonstrate the potential of azido-substituted carbon

Ultrasound-assisted Cu(I)-catalyzed azide-alkyne click cycloaddition as polymer-analogous transformation in chitosan chemistry. High antibacterial and transfection activity of novel triazol betaine chitosan derivatives and their nanoparticles-mediated CuAAC between propargylic ester of betaine and azido chitosan derivative proceeds fast in water under

Making endo-cyclizations favorable again: A conceptually new synthetic approach to benzotriazoles via azide group directed lithiation/cyclization of 2-azidoaryl bromides in situ from 2-azido-aryl bromides. The scope of the reaction is illustrated using twenty-four examples

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