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isopropyl-
Synthesis, stereochemistry, and antimicrobial evaluation of t(3)-isopropyl-r(2), c(6)-di-2'-furanylpiperidin- 4-one and its deri
      
coli BL-21 (DE3) were induced by isopropyl-β-thiogalactopyranoside (IPTG), and then expressed.
      
coli) by isopropyl-β-D-thiogalactopyranoside (IPTG) inducement.
      
Pretreatment of plant seeds with kartolin-4 (o-isopropyl-N-2-hydroxyethyl carbamate), a preparation with cytokinin activity, reduced the dehydration-induced inhibition of enzymatic activity.
      
Reaction of 2-Isopropyl-5,6-benzo-1,3,2-oxazaborepane with Acetonitrile
      
2-Isopropyl-1,3-dioxolane is oxidized to the corresponding monoester in quantitative yield, and the 2-phenyl derivatives yield benzaldehyde.
      
Isobutyraldehyde in the Synthesis of Isopropyl-substituted 4H-Pyrans, 1,4-Dihydropyrano[2,3-c]pyrazole, 1,4-Dihydropyridines, an
      
Nitration of d-tartaric acid, followed by treatment of the resulting dinitrotartaric acid with ammonia and aldehydes gave 2-phenyl-, 2-(2-pyridyl)-, 2-isopropyl-, and 2-isobutylimidazole-4,5-dicarboxylic acids.
      
Reaction of 1-(4-methoxyphenyl)-3-isopropyl-5-(4,6-diphenylpyrimidin-2-yl)formazan with nickel nitrate in acid medium yields N'-(4,6-diphenylpyrimidin-2-yl)-2-methylpropanoic hydrazide.
      
1-Aryl-2,2-dibromobutan-1-ones react with zinc and dialkyl arylmethylene- or isobutylidenemalonates to give dialkyl 2-aroyl-3-phenyl(isopropyl)-2-ethylcyclopropane-1,1-dicarboxylates which are formed mainly as Z isomers.
      
Comparison with the data on solvent effect on the equilibrium between 2-isopropyl-5-methoxy-1,3-dioxane epimers suggests that the formation of H-complexes is controlled by electronic and conformational factors.
      
An analog of 5α-hydroxyecdysteroids having an isoxazole ring in the side chain was synthesized starting from pregnenolone through intermediate 20-hydroxy-20-(3-isopropyl-4,5-dihydroisoxazol-5-yl) derivative.
      
Iodination of N-isopropyl- and N-benzyl-2-(2-cyclohexenyl)anilines gave the corresponding 1-iodo-hexahydrocarbazoles which underwent quantitative isomerization into 3-iodo-2,4-propano-1,2,3,4-tetrahydro-quinolines.
      
The thermodynamic parameters of the equilibrium formation of H-complex with 2-isopropyl-5-phenyltetrazole were determined.
      
Mass spectra of previously unknown isomeric 1-isopropyl-3-methoxy-2-methylsulfanylpyrrole, 5-methoxy-2,2-dimethyl-6-methylsulfanyl-2,3-dihydropyridine, and 3-methoxy-7-methyl-2-methylsulfanyl-4,5-dihydro-3H-azepine were studied for the first time.
      
coli strain M15 and the recombinant strain was induced to express by the optimum inducer (0.5 mM isopropyl-β-D-thiogalactopyranoside).
      
X-ray diffraction investigation of 1-phenyl-3-isopropyl-5-(benzothiazol-2-yl)formazan
      
The crystal structure of 1-phenyl-3-isopropyl-5-(benzothiazol-2-yl)formazan is investigated using X-ray diffraction.
      
Quantum-chemical predictions of the formation of H-bonds between the N-phenyl-N'-isopropyl-p-phenylenediamine and N,N'-diphenyl-
      
Time resolve study on isopropyl-ether porphyrindiol
      
 

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