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51.
L. G. Voskressensky T. N. Borisova L. N. Kulikova A. V. Varlamov 《Chemistry of Heterocyclic Compounds》2007,43(7):913-918
The interaction of 7-trifluoroacetyltetrahydropyrrolo[1,2-c]pyrimidine with acetylenedicarboxylic ester (DMAD) and ethyl propiolate
in acetonitrile and alcohols has been studied. It was established that DMAD splits pyrrolopyrimidine at the aminal fragment
in acetonitrile and methanol with the formation of 1-H-and 2-(N-dimethoxycarbonylvinyl-N-methyl)aminoethyl-1-methoxymethyl-3-methyl-5-trifluoroacetylpyrroles.
In acetonitrile ethyl propiolate splits pyrrolopyrimidine both at the aminal fragment and at the C(3)-N(2) bond (Hofmann reaction), but in ethanol only at the C(3)-N(2) bond with the formation of 2-propenylpyrroles.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 1082–1087, July, 2007. 相似文献
52.
In the enantioselective esterification of racemic naproxen with 4(2-hydroxyethyl) morpholine by Lipase MY in organic solvents,
a productivity improvement of the desired (S)-naproxen ester from 0.42 to 0.72 mM at the reaction time of 130 h was observed,
when the surfactantbis (2-ethylhexyl) sodium sulfosuccinate (AOT) was added in the reaction mixture. The presence of a small amount of exogenously
added water dramatically activated the enzyme in AOT/cyclohexane-reversed micelles. Desorption of the surfactant molecule
from the enzyme mass and solubilization of the enzyme into reversed micelles were used to elucidate an existing maximum of
the initial rate of (S)-naproxen synthesis with the water content. Moreover, the effects of alcohol and surfactant concentration
on the enzyme activity are reported. 相似文献
53.
Molecular routes to metal oxides has become an area of intensescientific interest due to the technological relevance of thesematerials. Molecular routes are proving important as a result ofthe possibility to control the physical and chemical propertiesof the final materials.We have chosen to study non-hydrolytic methods, namely esterelimination reactions between two prototypical molecularprecursors metal alkoxides, M(OR)n, and metal carboxylates, M(O2CR)n, to synthesize metal oxides:
This method allows for the synthesis of pure metal oxides bycomplete elimination of the organic supporting ligands withconcomitant formation of M-O-M bridges.Furthermore, incomplete esterelimination can lead to isolation of molecular clusters asintermediates which can also be used as building blocks for theformation of metal oxides with controlled microstructure.Here we report a series of reactions between Sn and Si alkoxidesand carboxylates designed to gain further insight into thefactors governing ester elimination reactions. By choosingcompounds with varying coordination environments and stericaccessibility we have devised a set of criteria which shouldallow for successful ester elimination between metal alkoxide andcarboxylate compounds. Furthermore we have also shown theability of ester elimination derived molecular clusters withspecific microstructure to be used in the synthesis of bulkmaterials retaining the structural attributes of the precursor cluster. 相似文献
54.
Wen Wei Lai Teh Chou Chang 《Journal of polymer science. Part A, Polymer chemistry》1995,33(7):1075-1083
A series of crosslinkable thermotropic liquid crystalline poly(ether-ester)s and copoly(ether-ester)s was prepared. All of the polymers were crosslinked by thermal treatment or photo-irradiation upon heating. The thermal stability and thermal crosslinking reaction of these polymers were investigated. These polymers also could be crosslinked by copolymerization with vinyl monomers, such as styrene or methyl methacrylate. The crosslinked polymers exhibited thermotropic liquid crystalline behavior after softening by heating. The phase behavior of linear polymers and crosslinked polymers was studied by differential scanning calorimetry (DSC) and an optical polarizing microscope equipped with a heating stage. © 1995 John Wiley & Sons, Inc. 相似文献
55.
56.
Cure kinetics of a cobalt catalysed dicyanate ester monomer in air and argon atmospheres from DSC data 总被引:1,自引:0,他引:1
A kinetic analysis of the cyclotrimerisation reaction of a dicyanate ester monomer catalysed by cobalt(II) acetylacetonate and nonylphenol in air and argon atmospheres has been carried out by differential scanning calorimetry (DSC). Dynamic and isothermal DSC scans as well as the glass transition temperature are the experimental data obtained. From isothermal scans a higher cyanate conversion in air than in argon was obtained. The cyanate conversions are satisfactorily described with a second-order kinetic equation in the kinetically controlled region, and by m-order (m<1) equation after vitrification is reached. Activation energies determined by different procedures agree among them, showing slightly higher values in argon than in air. 相似文献
57.
Akiko Saito Mana Emoto Akira Tanaka Yuki Doi Kazuaki Shoji Yoshiyuki Mizushina Hiroshi Ikawa Hiromi Yoshida Nobuyasu Matsuura Noriyuki Nakajima 《Tetrahedron》2004,60(52):12043-12049
A simple method for the synthesis of procyanidin B3 substituted with a galloyl group at the 3 and 3″ position is described. Condensation of a benzylated catechin-3-O-gallate electrophile with a nucleophile, catechin and catechin-3-O-gallate, proceeded smoothly and stereoselectively to afford the corresponding dimer gallates, procyanidin B3-3-O-gallate and procyanidin B3-3,3″-di-O-gallate, in good yields. Further, their antioxidant activities on UV-induced lipid peroxide formation, DPPH radical scavenging activity and inhibitory activity of DNA polymerase were also investigated. Among three procyanidin B3 congeners (procyanidin B3, 3-O-gallate and 3,3″-di-O-gallate), the 3,3″-di-O-gallate derivative showed the strongest antioxidant and radical scavenging activity. Interestingly, the 3-O-gallate derivative was the strongest inhibitor of mammalian DNA polymerase with IC50 value of 0.26 μM, although it showed the weakest antioxidant and radical scavenging activity. It became apparent that the presence of a galloyl group at the C-3 position in the proanthocyanidin oligomer was very important for biological activity, however, the antioxidant activity of these compounds was not parallel to the DNA polymerase inhibitory activity. 相似文献
58.
Nan Yan FU Mei Li PANG Yao Feng YUAN Ji Tao WANG* Department of Chemistry National Key Laboratory of Elemento-organic Chemistry Nankai University Tianjin 《中国化学快报》2002,13(10)
A highly efficient catalyst indium (III) tribromide is used to synthesize 5-alkoxy- carbonyl-4-hydrocarbyl-3,4-dihydropyrimidin-2(1H)-ones by a three-component coupling of β-keto ester, aldehydes and urea through improved Biginelli reaction. 相似文献
59.
采用齐格勒-钠塔催化剂使丙烯催化聚合得到聚丙烯。聚丙烯树脂本身具有优良的性能,如机械强度好,易加工成型,质量轻,成本低等,但也存在一些缺陷,如由于聚丙烯结构中存在叔碳原子,在造粒加工、贮存和使用过程中,易受热、光、氧等的作用而降解,导致材料的性能降低。为了抑制和延缓聚丙烯的氧化降解,需要在造粒阶段加入抗氧剂。本文以一种聚丙烯树脂样品为研究对象,采用溶剂抽提法提取有机添加剂,并用柱层析法对添加剂进行了分离;利用EI-MS分析了添加剂的组成,其中通过谱图解析,鉴定出添加剂中含有硫酯类抗氧剂-硫代二丙酸二(十四)酯(DMTP),并用此类常用化合物进行了验证,分析结果对树脂牌号的开发具有指导意义。 相似文献
60.
Takashi Iizawa Kazuaki Nishiyama Tadatomi Nishikubo 《Journal of polymer science. Part A, Polymer chemistry》1993,31(2):443-450
4-Acetoxy-2-cyclohexenone (ACH) and 2-cyclohexenone-4-yl methacrylate (CHM) were obtained from the condensation reaction of 4-bromo-2-cyclohexenone (BCH) with acetic acid and methacrylic acid using 1,8-diazabicyclo-[5,4,0]-7-undecene (DBU), respectively. Poly(2-cyclohexenone-4-yl methacrylate) ( P-1 ) containing acid-sensitive 2-cyclohexenone-4-yl group was prepared from the radical polymerization of CHM and the esterification of poly(methacrylic acid) with BCH using DBU. Furthermore, P-1 and CHM copolymers ( P-2 and P-3 ) were easily synthesized from the radical polymerization of methacrylic acid and comonomers in dimethylsulfoxide using 1 mol % of 2,2′-azobis (isobutyronitrile) followed by esterification of the resulting polymers with BCH using DBU by one-pot method. The deprotection reaction of ACH and P-1 was carried out in dichloromethane using an acid catalyst. The reaction proceeded smoothly in solution to give phenol and the corresponding carboxylic acid. Therefore, the 2-cyclohexenone-4-yl group is a useful protecting group for carboxylic acids, because the protection and deprotection reactions are very easy. In the case of polymer films, however, the acid was trapped by carbonyl group on the 2-cyclohexenone-4-yl group, and did not cause the deprotection reaction. © 1993 John Wiley & Sons, Inc. 相似文献