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Azide pre-click modification of chitosan: N-(2-azidoethyl)chitosan of the reduction product with sodium azide. The course of the formation of the Schiffbase (this step is determining

Thermochemistry of organic azides revisited Dedicated to Prof. Ch. Rüchardt on the Occasion of His 85th Birthday© 2014 Elsevier B.V. Highly pure samples of 4-nitro-phenyl azide, 1-octyl azide and 1 decyl-azide

Thermochemistry of organic azides revisited Dedicated to Prof. Ch. Rüchardt on the Occasion of His 85th Birthday© 2014 Elsevier B.V. Highly pure samples of 4-nitro-phenyl azide, 1-octyl azide and 1 decyl-azide

Synthesis, structure, and the energetic properties of tetraazidopyridine-4-carbonitrile with sodium azide was used to obtain tetraazidopyridine-4-carbonitrile, the structure of which was studied

Synthesis of tetrazolodiazepines by a five-centered four-component azide Ugi reaction. Scope and limitationsTetrazolo[1,5-a][1,4]benzodiazepines were obtained by an efficient azide five-centered four

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 was obtained in high yield by azidation of 4,6-dichloro-N-(4,6-dichloro-1,3,5-triazin-2-yl)-1,3,5-triazin-2

New copper-containing catalysts based on modified amorphous silica and their use in flow azide—alkyne cycloaddition
synthesized in the flow regime showed higher activity in the catalytic cycloaddition of azides to alkynes than

Three-component reaction of ketals, isonitriles, and trimethylsilyl azide-component reaction of ketals, isonitriles, and trimethylsilyl azide led to 1,5-disubstituted tetrazoles in moderate

4-(Dimethylamino)Pyridinium Azide in Protic Ionic Liquid Media as a Stable Equivalent of Hydrazoic AcidWe report a procedure for the multigram synthesis of 4-(dimethylamino)pyridinium azide, a stable

Synthesis of blue light emitting heterocyclesviacyclization of 2-pyridine derived 4-azido-r1,2,3-triazoles with sodium azide permits the preparation of target triazoles isolated in up to 92% yield. Subsequent thermal

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