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Aequationes mathematicae - Given a set $$T\subset (0, +\infty )$$ , a function $$c:T\rightarrow \mathbb R$$ and a real number p we study continuous solutions $$\varphi $$ of the simultaneous...  相似文献   
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In a route towards enantiomerically enriched 1-(β-hydroxypropyl)indoles, which are potentially useful building blocks for high value-added chemicals synthesis, a kinetic resolution approach by means of lipase-catalyzed enantioselective acylation as well as hydrolysis/methanolysis has been elaborated for the first time. The enzymatic resolution of chiral N-substituted indole-based sec-alcohols was successfully accomplished, yielding both enantiomeric forms of the employed derivatives with up to >99% enantiomeric purity via an enantioselective transesterification under mild reaction conditions. The most selective resolutions were obtained using fungal (CAL-B and TLL) and bacterial (PFL and BCL) lipases and vinyl acetate as the acyl?group donor. The synthetic protocol described herein is very simple, user-friendly and efficient, thus paving the way for future access towards more complex compounds of this type. The absolute configurations of novel enantiomeric derivatives, and thus stereoselectivity of the described enzymatic reactions were confirmed by application of CDA-based NMR methodology and single-crystal X-ray diffraction analysis.  相似文献   
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In the paper, the results of investigation concerning the influence of 0.3% addition of hydroxypropyl methylcellulose (MC) of 40 and 70 Pa s viscosity on the hydration process of main clinker phases C3S and C3A are presented. The course of hydration is documented using microcalorimetry, and formed phases were identified by XRD. The research indicated that methylcellulose inhibited the hydration process of clinker phases, analysed both, separately and in their mixture. Moreover, it was found that the presence of MC admixture also led to the reduction in calcium sulphate dihydrate reactivity in the system.  相似文献   
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The design, stereo-, and enantioselective synthesis and activity prediction of aminophosphonic acids as new leucine aminopeptidase inhibitors will be discussed.  相似文献   
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The synthesis of six analogues of the potent thymidylate synthase (TS) inhibitor N -[4-[ N -[(3,4-dihydro-2-methyl-4-oxo-6-quinazolinoyl)-methyl]- N -prop-2-ynylamino]benzoyl]- L -glutamic acid 2 is described in which the glutamic acid residue has been replaced by DL -aminophosphonic acids. New antifolates were tested as inhibitors of TS isolated from mouse L1210 leukemic cells as well as inhibitors of growth mouse leukemic L5178Y cells. In general these modifications result in compounds that are considerably less potent than 2 as TS inhibitors with K i 's 0.17-1.10 w M. Very poor solubility in water limited their proper assay of growth cells inhibition.  相似文献   
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