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双二茂铁基烷酰化衍生物的还原反应 总被引:1,自引:0,他引:1
二茂铁甲烷,2,2-双二茂铁丙烷,2,2-双二茂铁基丁烷,2,2-双二茂铁基戊烷与乙酸酐、丙酸酐、正丁酸酐通过傅氏酰基化反应生成一系列双二茂铁基烷的酰化衍生物,再经LiAlH_4还原得到318个相应的α-羟基双二茂铁烷衍生物。文中并对它们的红外光谱和~1H NMR谱性质进行了研究。 相似文献
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双(甲基二茂铁基)代烷羟的合成 总被引:1,自引:0,他引:1
二茂铁衍生物在复合固体火箭推进剂中用作燃速催化剂,但其挥发性和迁移性较大,直接影响储存或使用时导弹的弹导性能。本文报导三种新型燃速催化剂:双(甲基二茂铁基)甲烷,2,2-双(甲基二茂铁基)丙烷和2,2-双(甲基二茂铁基)丁烷的合成和表征。小型试验表明其催化活性、挥发性及迁移性能均优于国内目前使用的叔丁基二茂铁。 相似文献
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以2-二茂铁基苯并咪唑(2)为原料,合成了1-甲基-2-二茂铁基-3-乙基苯并咪唑碘盐(4)和六氟磷酸盐(5);甲酰化的2,2-双二茂铁基丙烷(6)与邻苯二胺在甲醇作溶剂,回流,碘催化下反应,得到2-[1’-(2-二茂铁基丙烷-2-基)二茂铁-1-基]苯并咪唑(7),以7为原料合成了1-甲基-2-[1’-(2-二茂铁基丙烷-2-基)二茂铁-1-基]-3-乙基苯并咪唑碘盐(9)和六氟磷酸盐(10).电化学分析表明所得的盐化合物中,与苯并咪唑阳离子直接相连的二茂铁的氧化电位相对2和7均产生了较大正移.对化合物4的单晶结构进行了解析,晶体结构中存在π-π堆积.UV-Vis吸收光谱表明所得盐化合物具有光致电荷迁移现象.DSC-TG(差示扫描量热-热重)测试表明碘盐4对高氯酸铵(AP)热分解有较好催化效果. 相似文献
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设计并合成了3个二取代和三取代的二茂铁-噻吩、二茂铁-联噻吩吡啶盐类化合物: 碘化(E,E)-N-甲基-2,4,6-三{2-[5-(2-二茂铁乙烯基)噻吩-2-基]乙烯基}吡啶盐、 碘化(E,E)-N-甲基-2,6-二{2-[5’-(2-二茂铁乙烯基)-2,2’-联噻吩-5-基]乙烯基}吡啶盐、碘化(E,E)-N-甲基-2,4,6-三{2-[5’-(2-二茂铁乙烯基)-2,2’-联噻吩-5-基]乙烯基}吡啶盐。初步研究了这些化合物的电化学性质,结果表明,该类多取代二茂铁吡啶盐具有很好的氧化-还原可逆性,是潜在的电化学分子材料。 相似文献
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报道了旋光性的顺式-2,2-二甲基-3-(2,2-二氯乙烯基)环丙烷羧酸(谷称顺式二氯菊酸)类杀虫剂光学纯度的色谱分析方法。光学活性杀虫剂的顺式-2,2-二甲基-3-(2,2-二氯乙烯基)环丙烷羧酸先与氯化亚砜生成酰氯,一财与S(-)-a-甲基苄胺作用,生成顺式-2,2-二氯-3-异丁烯基环丙烷羧酸非对映异构体的酰胺,经薄层色谱纯,用高效液相色谱进行分析,即可确定中间体的光学纯度。光学纯度一定的中间体经合成至最终产物,其光学纯度保持不变。 相似文献
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The corresponding diamides were obtained from reaction of cis-3-carboxy-2,2-dimethylcyclobutylacetic acid (pinic acid) and of cis/trans-3-(carboxymethyl)-2,2-dimethylcyclobutylacetic acid (homopinic acid) dichlorides with two equivalents of 5-bromo-, 4-chloro-, and 4,5-dimethoxyanthranilic acids. Treatment of them with formamide leads to the formation of the corresponding 2,2-dimethyl-3-[4(3H)-oxo-2-quinazolinyl]methyl-1-[4(3H)-oxo-2-quinazolinyl]cyclobutanes and 2,2-dimethyl-1,3-di[4(3H)-oxo-2-quinazolinylmethyl]cyclobutanes. 相似文献
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Veli-Matti Mukkala Christian Sund Marek Kwiatkowski Paavo Pasanen Marita Hgberg Jouko Kankare Harri Takalo 《Helvetica chimica acta》1992,75(5):1621-1632
Twelve heteroaromatic complexing agents 9a–I were synthesized with the purpose to develop suitable labels for time-resolved luminescence-based bioaffinity assays. The relative luminescence yields, excitation maxima, and emission decay constants of their europium(III) and terbium(III) chelates were determined. According to these results, 2,2′,2″,2?-[(2,2′-bipyridine-6,6′-diyl)bis(methylenenitrilo)]tetrakis (acetic acid) ( 9e ) and 2,2′,2″,2?-[(2,2′:6′,2″-terpyridine-6,6″-diyl)bis(methylenenitrilo)] tetrakis(acetic acid) ( 91 ) are the most promising agents. 相似文献
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The chemical reduction of 4,4′-dinitrostilbene-2,2′-disulfonic acid with titanium(III) chloride, chromium(II) sulfate, and vanadium(II) sulfate and the polarographic reduction of 4,4′-dinitrostilbene-2,2′-disulfonic acid were studied. Conditions for analytical use of these reactions were found. 相似文献
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Edwin G IJpeij Felix H Beijer Henricus J Arts Claire Newton Johannes G de Vries Gert-Jan M Gruter 《The Journal of organic chemistry》2002,67(1):169-176
Because of the promising performance in olefin polymerization of 2,2'-bis(2-indenyldiyl)biphenyl zirconium dichloride, we developed a new and broadly applicable route to 2,2'-bis(2-indenyl)biphenyl derivatives. Reaction of the known 2,2'-diiodobiphenyl (26) with the new 2-indenyl boronic acid (23) did not result in the desired 2,2'-bis(2-indenyl)biphenyl (10); instead an isomer thereof, (spiro-1,1-(2,2'-biphenyl)-2-(2-indenyl)indane) (27), was obtained. It was found that compound 10 could be made via a palladium-catalyzed reaction of 2,2-biphenyldiboronic acid (31) with 2-bromoindene (21) under standard Suzuki reaction conditions. However, the yield of this reaction was low at low palladium catalyst loadings, due to a competitive hydrolysis reaction of 2,2-biphenyldiboronic acid (31). HTE techniques were used to find an economically viable protocol. Thus, use of the commercially available 1.0 molar solution of (n-Bu)(4)NOH in methanol with cosolvent toluene led to precipitation of the pure product in a fast and clean reaction, using only 0.7 mol % (0.35 mol % per C-C) of the expensive palladium catalyst. 相似文献
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F. M. Avotin'sh M. V. Petrova A. Ya. Strakov 《Chemistry of Heterocyclic Compounds》2001,37(10):1241-1243
The corresponding diamides have been synthesized by the interaction of the diacid chlorides of cis-2,2-dimethyl-3-carboxycyclobutaneacetic acid (pinic acid) and cis-2,2-dimethylcyclobutane-1,3-diacetic acid (sym-homopinic acid) with two equivalents of anthranilic acid. Treatment of the diamides with formamide gave 2,2-dimethyl-1-[4(3H)-quinazolinon-2-yl]methyl-3-[4(3H)-quinazolinon-2-yl]cyclobutane and 2,2-dimethyl-1,3-di[4(3H)-quinazolinon-2-ylmethyl]cyclobutane respectively. 相似文献
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Peter Kasák 《Tetrahedron letters》2004,45(4):791-794
The first preparation of enantiomerically pure 1,1′-binaphthyl-2,2′-diboronic acid (by resolution) is reported. Optimization of the cross-coupling conditions was found to be crucial to achieve good yields in Suzuki arylation in approaches from both 2,2′-diiodide or 2,2′-diboronic acid (52-56%, with model p-tolyl reagents). Stereochemical results in these reactions were dramatically different: almost complete racemization starting from the 2,2′-diiodide versus complete conservation of stereogenic information from the 2,2′-diboronic acid. This novel synthetic approach, a stereoconservative Suzuki arylation of the diboronic acid, should be a valuable method for the synthesis of a new group of 2,2′-diarylated (including functionalized) binaphthyl derivatives. 相似文献
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V. P. Sheverdov V. V. Bulkin O. E. Nasakin V. A. Tafeenko 《Russian Journal of General Chemistry》2004,74(1):83-85
Oxidation of 3-(2,2-dialkylhydrazino)-1,1,2,2-tetracyano-5-R-cyclopentanes were converted into 3-(2,2-dialkylhydrazono)-1,1,2,2-tetracyano-5-R-cyclopentanes by treatment with potassium permanganate in a sulfuric acid or acetic acid solution and into 1-dialkylamino-5,5,6,6-tetracyano-4-R-piperidin-2-ones by treatment with nascent HOCl or HOBr. 相似文献
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Shigekazu Yamazaki 《合成通讯》2013,43(17):2210-2218
4,4′-Dicarboxy-2,2′-bipyridine was synthesized quantitatively by chromium(VI) oxide-mediated oxidation of 4,4′-dimethyl-2,2′-bipyridine or 4,4′-diethyl-2,2′-bipyridine with periodic acid as the terminal oxidant in sulfuric acid. 5,5′-Dicarboxy-2,2′-bipyridine and 6,6’-dicarboxy-2,2′-bipyridine were also synthesized by the method from the corresponding dimethyl bipyridines in excellent yields. 4,4′,4″-Tricarboxy-2,2′:6′,2″-terpyridine was obtained in 80% yield from 4,4′,4″-triethyl-2,2′:6′,2″-terpyridine, and 4,4′,4″,4′″-tetracarboxy-2,2′:6′,2″:6″,2′″-quaterpyridine was obtained in 72% yield from 4,4′,4″,4′″-tetraethyl-2,2′:6′,2″:6″,2′″-quaterpyridine by the same procedure. 相似文献