利用二进样条小波模极大方法消除毛细管电泳信号噪声的研究

根据毛细管电泳信号中噪声与真实信号的模极大值特性之间存在较大差异的特点，提出了一种利用二进样条小波模极大值法去噪的方法研究了信号的半峰宽、不同信噪比以及阈值的选取对去噪结果的影响，并对模拟含噪信号和含噪毛经电泳信号去噪前后的结果进行了比较，实验结果表明，该法能效地消除谱带较宽的毛细管电泳等信号中存在的噪声。     

一种新的小波滤波方法在化学谱图信号滤噪中的应用

仪器分析测定中，噪声的存在往往影响分析的准确度和仪器的检出限。小波变换多分辨分析的特性使得它成为一种很好的滤噪方法。基于小波分解后信号与噪声的小波系数随尺度变化规律不同的特性，提出了一种新的滤波滤方法-空域相关法，即通过不同尺度上相关系数模值与小波系数模模值的比较，达到滤波滤的目的。本文提出的方法具有无需人为选定无需人为选定滤噪阈值和小波函数、方法简单、失真度小等优点，可以大在提高信号的信噪比。模拟数据和ICP-AES实验数据证明了该方法的有效性。     

自适应中值滤波用于色谱信号去噪的研究

在分析化学领域中，如何从被干扰的信号中有效去除噪声并恢复有用信号，具有重要的意义。此文从中值滤波基本概念出发，针对经典中值滤波器滑动窗口长度固定对信号去噪的影响，提出了自适应中值滤波器，通过对某元素色谱曲线进行去噪处理，并与移动均值法和小波变换法进行比较表明，此方法不仅能有效地滤除脉冲和高斯噪声，而且使色谱峰的边缘得到良好保护，从而提高了色谱数据分析的精确性。     

二进小波变换极大模法用于分析化学信号的滤噪

实验数据的滤噪在分析化学领域中具有重要的意义。小波变换技术具有很强的信号分离能力，容易把随机噪声从信号中分离出来，从而提高信号的信噪比。本文使用滤噪方法不同于传统离散小波变换方法，而是通过引入二进小波变换和李氏指数的概念，根据噪声与有用信号的极大模截然不同的特征，实现信号滤噪。实验数据的仿真结果研究也证明该方法的可行性。     

小波包去噪信号的分形特征

将分形理论与小波包滤波相结合，用盒维数的大小来评判信号曲线的滤波情况。随着小波包分解尺度的增大，滤波后信号曲线的盒维数逐渐减小，并最后趋于稳定值。因此可以根据盒维数-分解尺度曲线来选择最佳分解尺度。对仿真含噪信号进行了滤波实验，结果表明：即使在信噪比低至0．5时仍能得到较好的结果，并且该法用于毛细管电泳实验数据的处理结果同样令人满意。     

小波变换法在X射线能谱去噪声中的应用

阐述了二进小波变换法的去噪声原理和方法,并将其应用于X射线能谱分析中噪声的去除。实验结果表明,该去噪方法能够解决传统平滑方法的滑方法的不足,改善X射线能谱的定性、定量分析结果。     

基于小波的恒电量瞬态响应信号的滤波处理

利用小波变换的阈值法对恒电量响应信号进行滤波处理, 同时与传统的时域和频域的滤波方法进行分析比较, 并且讨论了小波变换的分解层数对恒电量响应信号滤波效果的影响. 结果表明, 利用小波变换可以在时域和频域同时对恒电量响应信号取得良好的去噪效果. 这不仅能提高时域曲线拟合的精度, 还大大地提高了恒电量频谱解析的可靠性. 在实际应用中, 小波变换的分解层数取5～7层可以收到满意的效果.     

基于提升格式的小波变换用于处理化学信号

将提升haar小波变换应用于对不同类型含高噪声化学信号的处理,提出1种用于高噪声化学信号中滤除噪声的快速新方法——提升小波滤噪法,并使之与重叠峰分辨技术联用;以优选的小波分解层数对低信噪比的分析化学信号进行基于提升格式的小波变换处理,取得满意的结果;方法简单、快捷、准确、易行．运算速度是传统小波变换的一半,对高噪声化学信号的处理结果信噪比提高几百倍,峰位置相对误差小于1．5％;应用于氨基酸体系毛细管电泳检测信号的处理,有效降低了实验噪声的影响,分辨提取了难以察觉的信号．结果峰形变窄,峰高增加．大大提高了峰的分辨率．验证和显示了方法的可行性和优越性。     

分析化学信号在多尺度空间的滤噪

从多分辨率分析出发，结合离散正交小波变换(DWT)的理论，通过对各尺度下未抽取前的小波系数进行非线性滤波处理，达到在保护信号边缘的同时，有效实现白噪声及脉冲噪声的滤除。实验数据仿真结果研究也证明了该方法的可行性。     

分析化学窄带锐峰信号滤波新技术

窄带锐峰信号是指峰形狭窄、峰周围数据点极少的信号，采用常规滤波方法难以处理。本文提出了适合于这类信号的滤波新技术——Mexican Hat小波最小二乘法(MWLS)。它将原信号中的尖锐峰分离出来，以Mexican Hat小波构造拟合函数，根据最小二乘原理对各数据段进行拟合，再重构信号，以去除噪声。大量处理实践证明：该方法除噪能力强，滤波结果可靠，尖锐信号峰中的有用信息不会损失。即使对信噪比为1．5的高噪声锐峰信号仍能获得满意结果。     

A carbanion induced synthesis of highly congested pyrazole and imidazole containing heterocycles

An efficient approach to the synthesis of highly congested di, penta and hexacyclic pyrazoles as well as imidazole fragment containing novel heterocyclic molecule has been developed through a carbanion induced transformation of suitably functionalized 2H-pyran-2-ones, benzo[h]chromene and thiochromeno[4,3-b]pyrans. Due to the presence of fluorescence, we report their prime application metal sensor as off/on switching in ferric ions.     

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.     

Selective synthesis of 4,5-dihydroimidazo- and imidazo[1,5-a]quinoxalines via modified Pictet–Spengler reaction

An efficient tandem approach for the selective synthesis of 4,5-dihydroimidazo[1,5-a]quinoxalines 6a–g and imidazo[1,5-a]quinoxalines 7a–h by the reaction of 2-imidazolyl anilines 4a–c with aryl aldehydes 5a–k under mild reaction conditions is described. Introduction of electron releasing alkyl groups in substrates 4a–b was found to be instrumental for the success of the reaction.     

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%).     

Understanding the Diels-Alder reactivity of 1,2-azaborine analogues

The Diels-Alder reactivity of 1,2-heteroborines (H₄C₄B(H)X, X?=?NH, PH, AsH; O, S, Se) has been computationally explored by means of Density Functional Theory (DFT) calculations. The influence of the HB?=?X fragment on the reactivity of the system has been quantitatively analyzed in detail by means of the so-called Activation Strain Model (ASM) of reactivity. It is found that the interaction between these species and the dienophile is significantly stronger than that computed for their all-carbon isoelectronic counterpart, benzene. In addition, the strain energy plays a key role in the observed reactivity trends. The role of the aromaticity strength of these heteroarenes on the reactivity is also assessed.     

Synthesis of N-substituted carbazolones from α-iodo enaminones via Pd(0)-catalyzed intramolecular coupling under microwave irradiation

A variety of N-aryl and N-alkyl carbazolones were conveniently achieved in good to high yields via Pd₂(dba)₃-mediated intramolecular coupling of N-substituted α-iodo enaminones under microwave irradiation. The Pd(0)-catalyzed cyclization was found to proceed favorably with the more electron-deficient phenyl ring during the reactions involving unsymmetrical N,N-diaryl α-iodo enaminones. This unique property enables the construction of carbazolone skeleton containing nitro substituted benzenoid ring.     

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.     

Synthesis of substituted 2,4,5,6-tetrahydrocyclopenta[c]pyrazoles and 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles by intramolecular nitrilimine cycloaddition

Both substituted 2,4,5,6-tetrahydrocyclopenta[c]pyrazoles and 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazoles have been synthesized by the 3+2 intramolecular dipolar cycloaddition of nitrilimines to alkynes. This cyclization has been extended to more versatile 3-bromo derivatives by the use of alkynylbromides as dipolarophiles.     

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.