冠心病患者全血微量元素锌、铜、铁的分析

用原子吸收法测定５０例健康人、５２例冠心病患者全血微量元素锌、铜、铁的含量，并对５２例冠心病患者全血微量元素锌、铜、铁的含量及锌／铜比值，与其血脂总胆固醇（ＣＨ）、甘油三酯（ＴＧ）、高密度脂蛋白（ＨＤＬ）、低密度脂蛋白（ＬＤＬ）的浓度分别作线性相关分析。结果表明：（１）冠心病患者全血锌、铁、锌／铜比值均高于健康人（Ｐ＜０．０５），全血铜低于健康人（Ｐ＜０．０５）。（２）全血锌与ＨＤＬ呈负相关（Ｐ＜０．０１）、锌／铜比值与总胆固醇呈正相关（Ｐ＜０．０５），铁与ＬＤＬ呈正相关（Ｐ＜０．０１）．提示锌／铜比值增高及体内铁储存增加均可能是冠心病易患因素．     

产妇血及其新生儿脐带血中铁、锌、铜、硒含量的研究

选取包头市区正常产妇６８名及其所生新生儿作为研究对象。分娩后抽取产妇肘静脉血及新生儿脐动脉血，分析其血清中铁、锌、铜、硒的含量．研究结果揭示：新生儿脐带血清中铁、铜、硒的含量均高于产妇血清中的含量，铁与铜有显著性差异（Ｐ＜０．０５），硒的差异不显著（Ｐ＞０．０５）；而锌则相反，新生儿脐带血清中的含量低于产妇血清中的含量，二者有高度显著性差异（Ｐ＜０．０１）。产妇血清中Ｆｅ／Ｚｎ、Ｃｕ／Ｚｎ、Ｓｅ／Ｚｎ比值分别为３．８３、２．７８、０．０８；而新生儿脐带血清中Ｆｅ／Ｚｎ、Ｃｕ／Ｚｎ、Ｓｅ／Ｚｎ比值则各为９．５６、６．８０、０．１９，进一步说明新生儿脐带血清中的锌含量降低，其它元素含量增加。     

血清中Mo、Se、Mn、Cu、Zn与食管癌的关系探讨

通过对１８例食管癌患者以及８０例对照组血清中Ｍｏ、Ｓｅ、Ｍｎ、Ｃｕ、Ｚｎ的测定分析，发现食管瘤患者血硒含量明显低于对照组，二者之间有极显著性差异（Ｐ＜０．０１）。而血铜、铜／锌比值食管癌组明显高于对照组，差异有显著性（Ｐ＜０．０５）。Ｍｏ、Ｍｎ、Ｚｎ元素的含量在二组之间无显著性差异（Ｐ＞０．０５）．提示血清硒铜与食管癌有关。     

血液病与微量元素关系的研究

研究了血液病与微量元素的关系,发现再生障碍性贫血患者治疗前血清Ｃｕ升高（Ｐ〈０．０５）,缓解后Ｃｕ恢复正常。骨髓增生异常综合征（ＭＤＳ）中ＲＡ＋ＲＡＳ组Ｃｕ及Ｃｕ／Ｚｎ比值高,Ｚｎ值降低不明显;ＲＡＥＢ＋ＲＡＥＢ－Ｔ组Ｃｕ及Ｃｕ／Ｚｎ高,Ｚｎ值明显降低（Ｐ〈０．０５）。急性白血病、淋巴瘤、多发性骨髓瘤及慢粒患者血清Ｃｕ、Ｚｎ及Ｃｕ／Ｚｎ比值与对照组比较均呈显著差异（Ｐ〈０．０５￣０．０１）,而缓解     

胃癌病人发微量元素测定及其临床意义

对４３例胃癌病人测定了发中Ｚｎ、Ｃｕ、Ｆｅ、Ｍｎ、Ｃａ、Ｍｇ六种元素，结果：胃癌组发中Ｃｕ、Ｆｅｘ±ＳＤ值较健康对照组升高，Ｐ＜０．０５，有显著性差异．Ｚｎ、Ｃａ、Ｍｇｘ±ＳＤ值较健康组降低，Ｐ＜０．０５、＜０．０１、＜０．０１，差异有显著性和高度显著性．ＭＵｘ±ＳＤ值与健康对照组近似，Ｐ＞０．０５，差异无显著性．胃癌组Ｚｎ／Ｃｕ比值较健康对照组降低，Ｐ＜０．０１，差异高度显著性；胃癌组Ｚｎ／Ｆｅ比值与健康组近似，Ｐ＞０．０５，差异无显著性．Ｆｅ升高，Ｍｎ、Ｚｎ降低是胃癌的危险因素，Ｍｎ有抗癌抑癌作用，Ｆｅ、具有强烈催化自由基及过氧化反应的能力．发中微量元素测定可作为临床胃癌病人辅助诊断参考．     

尿毒症患者与血清八种元素含量关系的研究

检测了３７例尿毒症患者血清微量元素Ｆｅ、Ｃｕ、Ｚｎ和常量元素Ｋ、Ｎａ、Ｃａ、Ｍｇ、Ｐ的含量，并进行比较，探讨其相互关系，以期为尿毒症的发生发展及防治措施提供依据．结果发现尿毒症患者血清Ｋ、Ｐ、Ｍｇ极显著高于对照组（均Ｐ＜０．０１），而Ｎａ、Ｃａ、Ｚｎ、Ｃｕ、Ｆｅ及Ｎａ／Ｋ、Ｃａ／Ｍｇ则极显著低于对照组（均Ｐ＜０．０１），且Ｎａ／Ｋ、Ｃａ／Ｍｇ与肾实质受损程度呈负相关，提示Ｎａ／Ｋ、Ｃａ／Ｍｇ降低与尿毒症的发生发展过程有密切的关系．     

中风患者血清微量元素观察

采用原子吸收分光光度法测定８７例中风患者血清中Ｃａ、Ｍｇ、Ｚｎ、Ｃｕ、Ｆｅ含量，并与正常组作对比。结果表明：中风患者Ｚｎ、Ｆｅ降低，而Ｍｇ、Ｃｕ增高，Ｚｎ／Ｃｕ比值降低（Ｐ＜０．０５～０．０１）；而两组血清Ｃａ无统计学上的差别（Ｐ＞０．５０）。     

脊髓小脑变性疾病病人血清铜,锌,铝,铁含量的研究

脊髓小脑变性疾病（ＳＣＤ）的病因可能与遗传、神经生化紊乱、感染、微量元素平衡障碍及自由基损伤等因素有关，其中微量元素平衡障碍的研究具有重要意义。检测了ＳＣＤ中发病率较高的橄榄桥小脑萎缩症（ＯＰＣＡ）及晚发性小脑皮质萎缩症（ＬＣＣＡ）病人１５例血清中铜、锌、铝、铁等微量元素含量。发现病人比对照组铜明显降低，Ｐ〈０．０１；锌明显降低，Ｐ〈０．０１；铝明显升高，Ｐ〈０．０１；铁无明显差别。     

小儿支气管哮喘与免疫功能及微量元素关系的临床研究

通过临床对照研究,发现哮喘患儿血Ｔ淋巴细胞亚群Ｔ３、Ｔ４、Ｔ８及Ｔ４／Ｔ８比健康对照组显著低下（Ｐ＜０００５）,而总ＩｇＥ则显著升高。患儿血中必需微量元素Ｚｎ、Ｓｅ、Ｃｒ、Ｓｒ及宏量元素Ｂ、Ｍｇ比健康对照组显著降低,而Ｆｅ、Ｃｕ、Ｃａ、Ｖ、Ａｌ、Ｃｏ及有害元素Ｃｄ则显著升高（Ｐ＜００５）。结果表明,小儿哮喘与人体免疫缺陷、部分微量元素降低及有害微量元素升高密切相关。提示：提高人体免疫功能、调节微量元素代谢失衡对提高哮喘防治效果有重要意义。     

恶性骨肿瘤病人血清铜,锌测定

对１９名恶性骨肿瘤病人进行了血清铜、锌测定，与正常对照组进行比较，结果显示患病组血清铜２１．２±６．４４μｍｏｌ／Ｌ高于对照组的１４．２±３．６０μｍｏｌ／Ｌ（Ｐ＜０．０１），且铜／锌比值明显增高（Ｐ＜０．０１）。血清锌两组间差异无显著性意义。     

二氧化碳和丙烯直接合成甲基丙烯酸的NiPMo/TiO2催化剂的研究

用溶胶-凝胶法以磷钼酸(MPA)的镍盐溶液水解钛酸四丁酯制备了NiPMo/TiO2催化剂.使用ICP、 XRD、 TG-DTA、 IR、 TPD-MS和微反应技术研究了催化剂的化学组成、热稳定性、化学吸附性质和催化反应性能.杂多钼酸盐与TiO2通过O2-在TiO2表面发生了键合.在623 K下,杂多阴离子仍保持原有的Keggin结构.CO2在Lewis酸位Ni(Ⅱ)和Lewis碱位Ni-O-Mo的桥氧协同作用下生成CO2卧式吸附态Ni(Ⅱ)←O-(CO)←(O--Ni).丙烯有多种吸附态在催化剂上吸附.在563 K、 1 MPa和空速1500 h-1的反应条件下,丙烯的摩尔转化率为3.2%,产物MAA选择性为95%.     

α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles

A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives.     

Specific intramolecular aromatic CH insertion of diazosulfonamides

The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp³)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp²)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp²)?H and aliphatic 1,5- and 1,6-C(sp³)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp³)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp²)?H insertion.     

Toward new camptothecins. Part 6: Synthesis of crucial ketones and their use in Friedländer reaction

In the context of the preparation of camptothecin and luotonin A analogs, the synthesis of some key keto-precursors and their use in Friedländer condensation are described. This paper also focuses on the stability of these keto intermediates and emphasizes the major differences between indolizinones and pyrroloquinazolinones series. Noteworthy is also the report of some original structures isolated as by-products of some experiments.     

N-Heterocyclic carbene-palladacyclic complexes: synthesis,characterization and their applications in the C-N coupling and α-arylation of ketones using aryl chlorides

N-Heterocyclic carbene-palladacyclic complexes 3 were successfully achieved in a one-pot procedure under mild conditions. The structure of 3a was unambiguously confirmed by X-ray single crystal diffraction and it was an active catalyst in the Buchwald-Hartwig amination and α-arylation of ketones even at very low catalyst loadings (0.01?mol%).     

Iodine-mediated oxidative Pictet-Spengler reaction using terminal alkyne as the 2-oxoaldehyde surrogate for the synthesis of 1-aroyl-β-carbolines and fused-nitrogen heterocycles

An efficient iodine-mediated oxidative Pictet-Spengler reaction in dimethyl sulphoxide (DMSO) using terminal alkynes as the 2-oxoaldehyde surrogate for the synthesis of aryl (9H-pyrido[3,4-b]indol-1-yl)methanones is described. The scope of the protocol includes the total synthesis of Fascaplysin, Eudistomins Y₁ and Y₂. The methodology is extended for preparing pyrrolo[1,2-a]-quinoxaline and indolo[1,5-a]quinoxaline derivatives. The utility of 1-aroyl-β-carbolines was demonstrated by performing palladium-catalyzed β-carboline directed ortho-C(sp2)-H functionalization of the phenyl ring with thiomethyl (SMe) group using DMSO as source and for accessing 4-aryl-canthin-6-ones.     

CoFe2O4自形成磁性液体场致结构化对磁化的影响

The Langevin paramagnetic theory can’t describe the relation between magnetization of ferrofluids and applied magnetic field. The structuralization of ferrofluids, which is considered the main influence factor of the magnetization, is regarded. The part of magnetization works is deposited when the structure is forming. This action influences the magnetization of ferrofluids directly or indirectly. On the base of the “compressing” model, the Langevin function that usually describes the magnetization of ferrofluid is modified, and a well-fitted curve is obtained. An equation of the relation between the equivalent volume fraction after being “compressed” and the intensity of magnetic field is discovered, which approximately describes the process of magnetization. The relation between the approximate initial susceptibility and the volume fraction can be obtained from modified formula.     

Facile synthesis of bicyclic 1-arylpyrazol-5-ones

In this Letter, we described a facile method for constructing fused bicyclic 1-arylpyrazol-5-one ring system. We employed various methylene-containing carboxylic acids as the substrates and proved that the pyrazolone ring closure requires activated methylene group in intermediate II. Accordingly, a series of structurally diversified, fused bicyclic 1-arylpyrazol-5-ones was prepared in moderate to high yields using the requisite substrates.     

KMnO4-mediated oxidative CN bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

KMnO₄-mediated oxidative CN bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.     

Highly regioselective Buchwald–Hartwig amination at C-2 of 2,4-dichloropyridine enabling a novel approach to 2,4-bisanilinopyridine (BAPyd) libraries

The highly regioselective Buchwald–Hartwig amination at C-2 of the cheap and readily accessible reagent, 2,4-dichloropyridine with a range of anilines and heterocyclic amines is described. This new methodology is robust and provides a facile access to 4-chloro-N-phenylpyridin-2-amines on 0.25 mol scale. These intermediates undergo a further Buchwald–Hartwig amination at higher temperature to enable rapid exploration of the chemical space at C-4 and to provide a library of 2,4-bisaminopyridines.