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排序方式: 共有164条查询结果,搜索用时 15 毫秒
161.
Slana GB de Azevedo MS Lopes RS Lopes CC Cardoso JN 《Beilstein journal of organic chemistry》2006,2(1):1
Using new variations of anionic aromatic chemistry, the total synthesis of oxygenated brazanquinones (1a-1c), derived from beta-brasan, a natural product isolated from Caesalpina echinata, via carbamates 2a-2c is described. 相似文献
162.
Water-in-Oil-in-Water Double Emulsions as Protective Carriers for Sambucus nigra L. Coloring Systems
Liandra G. Teixeira Stephany Rezende ngela Fernandes Isabel P. Fernandes Lillian Barros Joo C. M. Barreira Fernanda V. Leimann Isabel C. F. R. Ferreira Maria-Filomena Barreiro 《Molecules (Basel, Switzerland)》2022,27(2)
The use of natural colorants is needed to overcome consumer concerns regarding synthetic food colorants′ safety. However, natural pigments have, in general, poor stability against environmental stresses such as temperature, ionic strength, moisture, light, and pH, among others. In this work, water-in-oil-in-water (W1/O/W2) emulsions were used as protective carriers to improve color stability of a hydrophilic Sambucus nigra L. extract against pH changes. The chemical system comprised water and corn oil as the aqueous and oil phases, respectively, and polyglycerol polyricinoleate (PGPR), Tween 80, and gum Arabic as stabilizers. The primary emulsion was prepared using a W1/O ratio of 40/60 (v/v). For the secondary emulsion, W1/O/W2, different (W1/O)/W2 ratios were tested with the 50/50 (v/v) formulation presenting the best stability, being selected as the coloring system to test in food matrices of different pH: natural yogurt (pH 4.65), rice drink (pH 6.01), cow milk (pH 6.47), and soy drink (pH 7.92). Compared to the direct use of the extract, the double emulsion solution gave rise to higher color stability with pH change and storage time, as corroborated by visual and statistical analysis. 相似文献
163.
Dr. Christian Paul Bold Dr. Daniel Lucena-Agell Dr. Dr. María Ángela Oliva Dr. José Fernando Díaz Prof. Dr. Karl-Heinz Altmann 《Angewandte Chemie (International ed. in English)》2023,62(5):e202212190
We describe the total synthesis of the macrodiolide C(13)/C(13′)-bis(desmethyl)disorazole Z through double inter-/intramolecular Stille cross-coupling of a monomeric vinyl stannane/vinyl iodide precursor to form the macrocycle. The key step in the synthesis of this precursor was a stereoselective aldol reaction of a formal Evans acetate aldol product with crotonaldehyde. As demonstrated by X-ray crystallography, the binding mode of C(13)/C(13′)-bis(desmethyl)disorazole Z to tubulin is virtually identical with that of the natural product disorazole Z. Likewise, C(13)/C(13′)-bis(desmethyl)disorazole Z inhibits tubulin assembly with at least the same potency as disorazole Z and it appears to be a more potent cell growth inhibitor. 相似文献
164.
Raul Quijada Jairton Dupont Dione Corrêa Silveira Mrcia S. Lacerda Miranda Rosngela B. Scipioni 《Macromolecular rapid communications》1995,16(5):357-362
This work reports a comparative study of the catalytic behaviour for a series of metallocenes derived from Ti, Zr, Hf and Nb, which after activation with methylaluminoxane can polymerize ethylene. Results show that the Zr metallocene with a (CH3)2Si Bridge presents the highest activity, and the metallocenes based on Hf and Nb do not show any significant activity under the tested conditions. 相似文献