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101.
Hans-Rainer Sagaster Gerhard Rbisch Achim Mehlhorn 《Advanced Synthesis \u0026amp; Catalysis》1987,329(6):1045-1051
Investigations on the Tautomerism of o,o'-Dihydroxy Azo Dyes of the Eriochrome Type Investigation of the u.v.-vis-, 1H- and 13C-n.m.r. spectra of the title substances and the isomers 3 and 3p at different pH-values and in different solvent mixtures as well as of O,O'-dimethyl derivatives of 2 and 3 show that in aqueous solution as well the monoanions as the trianions exist in the azo forms only. The dianions exist in dependence on the solvents as mixtures of tautomers. The results of PPP calculations for different prototropic structures are in good accordance with the experimental results. 相似文献
102.
103.
104.
Klaus Kirschke Gerhard Lutze Ernst Schmitz 《Advanced Synthesis \u0026amp; Catalysis》1984,326(3):367-373
Ring Opening and Substitution Reactions of 4,4-Dihalo-pyrazolin-5-ones with Nucleophiles 1-Aryl-4,4-dihalo-3-methyl-pyrazolin-5-ones ( 1a – c ) undergo ring opening with alkoxides and form alkyl 3-arylazo-2-halo-2-butenoats ( 2a – d ). Analogous reactions take place with ammonia and amines. 4-Nitro-phenoxide reacts with substitution of both halogens to the 4,4-bis(4-nitro-phenyl)-compound ( 5 ). Phenols are selectively orthobrominated by the title compounds 1a and b . 相似文献
105.
Gerhard W. Fischer Thomas Zimmermann Manfred Weissenfels 《Advanced Synthesis \u0026amp; Catalysis》1983,325(5):729-741
Pyrylium Compounds. XVIII. 2-Alkoxy-2H-pyrans from Tetra- and Pentasubstituted Pyrylium Salts Alkali alkoxides add regioselectively to 2,3,4,6-tetrasubstituted pyrylium salts 7 (R' H), affording high yields of colourless crystalline 2-alkoxy-2H-pyrans 9 . The latte are also formed simply on refluxing 7 in the corresponding alcohol with triethylamine as proton acceptor. 3,5-Dialkylsubstituted 2,4,6-triarylpyrylium salts react analogously. The 2H-pyran structure of the adducts obtained follows from their n.m.r., i.r., u.v. and mass spectra as well as from their reaction with tetracyanoethylene to cycloadducts of type 10 . Acids regenerate from 9 the original pyrylium cations, whereas reaction of 9 with nitromethane or ethyl cyanoacetate provides benzene derivatives. -- The novel starting pyrylium salts 7b--o are characterized by u.v./vis data and by transformation into the corresponding pyridine derivatives 相似文献
106.
107.
Investigations on Potato Pulp as a Dietary Fiber Source. Composition of Potato Pulp After Influence of Pectinases and Cellulases and Enzymatic Degradation of Starch. The composition of alcohol insoluble substances (AIS) of potato pulp have been investigated after succesive degradation with different pectolytic and cellulolytic enzymes followed by starch degrading enzymes. The pretreatment with pectinase/cellulase combinations has a significant influence on the amount and the properties of the residues after starch degradation. Furthermore the most important changes in the composition were found in the receiving residues after action of amylolytic enzymes. A correlation exists between the content of residual starch in the residues and the action of the cell wall degrading enzymes. The amount of residual starch correlates negatively with the intensity of cell wall degradation. The enzymatic susceptibility of starch depends on the damage of cell wall of potato pulp, especially on the degree of degradation of the cellulose. The water binding capacity decreases intensively after action of pectinase/cellulase combinations. The treatment with amylolytic enzymes causes only a negligible variation of the water binding capacity. 相似文献
108.
Jrg Hofmann Gerhard Just Wilhelm Pritzkow 《Advanced Synthesis \u0026amp; Catalysis》1991,333(1):67-71
The title compounds were prepared from 2,4-dioxohexahydro-triazine (DHT) and the corresponding acid chlorides in the presence of sulphuric acid. They are active acylating agents against piperidine in dioxane as the solvent. Only the diacyl derivatives of DHT with acyl chain lengths up to C6 react with aqueous solutions of sodium perborate forming the corresponding peroxy acids. 相似文献
109.
Flavins and Chinamoyl Derivatives in Relation to the Light-induced Leaf Opening in Albizia julibrissin In search of blue-light photoreceptors for light-induced leaf opening we isolated from the aqueous extract of Albizia julibrissin Durazz. two flavins by adsorption on XAD-4 and separation with HPLC. One sample was identified as riboflavin 1a. In the hydrolysate of the second flavin fraction we found another dimethylisoalloxazine with a C5-side chain. Furthermore we isolated the cinnamoyl derivatives 3-O-(4-hydroxy-trans-cinnamoyl) quinic acid 2 and 3-O-(3,4-dihydroxy-trans-cinnamoyl)-4-O-malonyl-quinic acid 3 which formed charge transfer complexes with the flavins in the XAD-fraction. As a model complex we examined the absorption behaviour of the complex between riboflavin and chlorogenic acid. Using the association constant, we calculated the absorption spectrum and could show that a complex between a flavin and a phenolic compound is a possible blue-light photoreceptor for the light-induced leaf opening in Albizia julibrissin. 相似文献
110.
Dr. Markella Konstantinidou Francesca Magari Fandi Sutanto Dr. Jörg Haupenthal Dr. Varsha R. Jumde Dr. M. Yagiz Ünver Prof. Dr. Andreas Heine Dr. Carlos Jamie Camacho Prof. Dr. Anna K. H. Hirsch Prof. Dr. Gerhard Klebe Prof. Dr. Alexander Dömling 《ChemMedChem》2020,15(8):680-684
Pharmacophore searches that include anchors, fragments contributing above average to receptor binding, combined with one-step syntheses are a powerful approach for the fast discovery of novel bioactive molecules. Here, we are presenting a pipeline for the rapid and efficient discovery of aspartyl protease inhibitors. First, we hypothesized that hydrazine could be a multi-valent warhead to interact with the active site Asp carboxylic acids. We incorporated the hydrazine anchor in a multicomponent reaction and created a large virtual library of hydrazine derivatives synthetically accessible in one-step. Next, we performed anchor-based pharmacophore screening of the libraries and resynthesized top-ranked compounds. The inhibitory potency of the molecules was finally assessed by an enzyme activity assay and the binding mode confirmed by several soaked crystal structures supporting the validity of the hypothesis and approach. The herein reported pipeline of tools will be of general value for the rapid generation of receptor binders beyond Asp proteases. 相似文献