共查询到19条相似文献,搜索用时 62 毫秒
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以对苄氧基苯酚,对苄基苯酚和对苯氧基苯酚作为底物,研究在无溶剂体系下,酪氨酸酶分别催化它们与邻氨基苯甲醚的反应。考察了在无溶剂体系下,以底物200μmol为当量,酶催化该类反应的最适水含量为30~35μL,加酶量为35~40mg,反应时间为24h,以此为反应条件酶促催化合成了2和3b,3a,产率30~50%,并讨论了反应机制。 相似文献
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苯酚钾及对位取代苯酚钾的电离势 总被引:2,自引:0,他引:2
在我们以前的研究工作中发现,酚类钾盐是很好的电荷给体,可以和顺丁烯二酸酐、三硝基苯以及醌类等电荷受体生成电荷转移(CT)络合物。表示分子的给电子能力的参数是分子的第一电离势(简称为电离势I_p)。对于苯酚的I_p值,近年来已有文献记载,但苯酚钾 相似文献
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为了获得新的活性化合物,以溴代四乙酰葡萄糖和对位以代苯酚为原料,溴化 四丁基铵为相转移催化剂,合成了18个对位取代苯酚氧甙类化合物,其产率为20. 0%。化合物结构经元素分析,IR,^1H NMR表征,化合物的生物活性经初步测定, 其中四种有抑制端粒酶活性。 相似文献
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Mannich反应是一类重要的有机化学反应,典型的Mannich反应是在酸催化下进行的。近年来,一些固体催化剂如AgNO_3、Cu_2X_2(X=C1、Br、I)、 CuCl_2、CuBr_2、Cu(OAC)_2等也被用于一些特殊的Mannich反应中,但有关报道不多。Al_2O_3作为Man-nich反应的催化剂未见文献报道。 1982年,陈光旭、徐秀娟等采用HCl-EtOH作催化剂,首次实现了芳香胺作为胺组分与甲醛和酮直接进行的Mannich反应,合成了一系列β-芳胺基酮: 相似文献
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Guizhou Yue Kaining Lei Hajime Hirao Jianrong Zhou 《Angewandte Chemie (International ed. in English)》2015,54(22):6531-6535
Asymmetric reductive Heck reaction of aryl halides is realized in high stereoselectivity. Hydrogen‐bond donors, trialkylammonium salts in a glycol solvent, were used to promote halide dissociation from neutral arylpalladium complexes to access cationic, stereoselective pathways. 相似文献
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Summary The isocratic HPLC analysis of hydroquinone and its derived ethers in cosmetic preparations, as described in the sixth Directive
95/32/EC of the European Commission, was investigated with a view to determining the fundamental validation parameters of
the technique.
The calibration lines are highly linear with coefficients of determination >0.9996; the slopes of the calibration equations
as well as the slopes normalised to the standard deviations indicate increased sensitivities for all compounds. The method
is very reproducible; both the repeatability and the intermediate precision confirm a system performance of <2% variation;
the limits of repeatability and intermediate precision are consistently <6% for every compound studied. The detection limits
correspond to concentrations of 0.03 and 0.02% (m:m) for hydroquinone and the derived ethers, respectively. Application of
the response factor calculation gives reliable results and signifies a practical and economic advantage when compared to laborious
calibration with several replicate standard injections. Comparison of the response factor and calibration techniques did not
reveal significant differences. The obviously insufficiently efficient extraction preceding chromatographic analysis might
constitute the only drawback of the method, especially when the concentrations applied border the allowable. 相似文献