Synthesis and Crystal Structure of N-cyclopropyl-9 -（3,4-dicholophenyl）- 1,2,3,4,5,6,7,8,9,10-decahydroacridine -1,8-dione under Microwave Irradiation

1 INTRODUCTION aryl or methyl group to the nitrogen atom of these compounds leads to enhanced activities of fluo- A lot of natural and synthetic compounds con- rescence[7, . Since the pyridine scaffold is included 8] taining acridine skeletons display interesting biolo- in decahydroacridine-1,8-dione, a question is whether gical and physical activities[1]. Acridinedione, for the same modification on the nitrogen atom of de- example, has been identified as antimalarial and cahydroacridine-1…     

Study of the reactions and reaction mechanisms of phosphine (Ph3P) and of phosphite ((PhO)3P) with sulphur (S8)

The reactions of sulphur with phosphine and phosphite were investigated by low-energy electron impact mass spectrometry and fast atom bombardment mass spectrometry. A previously reported mechanism of the Ph₃P–S₈ reaction was supported and a possible mechanism for the (PhO)₃P–S₈ reaction is proposed.     

Two New Xanthone Glycosides from Polygala tenuifolia

Two new xanthone glycosides,polygalaxanthone IV and V were isolated from the roots of Polygala tenuifolia Willd. Their structures were established as 6-O-[α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranosyl]-1-hydroxy-3,7-dimethoxyxanthone(polygalaxanthone IV), and 6-O-[α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranosyl]-1,3-dihydroxyl-7-methoxyxanthone (polyga-laxanthone V),respectively, on the basis of chemical and spectral evidence.     

多组分体系同时定性定量测定的逐步回归分析法

阐述了逐步回归分析法用于多组分体系同时定性定量分析的原理、实验及数据处理方法。分析了硝基酚类人工样、未知样及合成样。该法可用于仅知可能含有的组分范围的样品分析。     

用旋转园盘-园环电极研究碘酸盐阴极还原反应的机理

本文研究了低浓度的碘酸盐在硫酸介质中, 在铂电报上的电化学还原。用旋转盘环电极检测到了碘酸盐阴极还原的中间产物I_2及最终产物I~-。测定了电化学反应的动力学参数。最后提出了磺酸盐阴极反应的机理。     

手性螺环单磷配体在不对称氢甲酰化反应中的应用

为了进一步拓展具有螺二氢茚骨架的亚磷酸酰胺酯、亚磷酸酯、亚膦酸酯等手性螺环单磷配体在不对称反应中的应用范围, 研究了手性螺环单磷配体在铑催化苯乙烯衍生物的氢甲酰化反应中的选择性.     

Formation at low surfactant concentrations and characterization of mesoporous MCM-41

At low concentrations of cetyltrimethylammonium bromide,all silica-based mesoporous materials with hexagonal phase have been synthesized via interactions between self-assembled surfactant molecule aggregates and aniomc silicate polymers.The resulting materials are characterized by XRD,FT-IR,solid state 29Si MAS NMR,thermal analysis and N2 adsorption-desorption measurements.After soluble ions are removed,the interactors between surfactant micelles and silicate polymers are reorganized and then form mesostructures 1 he hexagonal framework is sonsistent with amorphous silica gel.The structures of materials depend on the synthesis conditions Hydrothermal process improves the interactions between molecules and increases the degree of framework silicon atom polymerization The.surface area and the mesopore volume of the material prepared at 100℃ increase by 87% and 71 %,respectively,compared with those obtained at room temperature.     

高效前沿分析的发展及在药物-蛋白结合研究中的应用

介绍了高效前沿分析方法的原理、特点、种类，综述了它在药物与蛋白结合研究中的应用及国内外研究概况；通过与高效液相色谱／前沿分析比较，阐明了毛细管电泳／前沿分析在药物蛋白结合研究中的优势；分析了在药物与蛋白结合研究中所采用的各种研究方法，通过与这些研究方法的比较，阐明了高效前沿分析的优越性及其广阔的应用前景，同时提出了在高效前沿分析方法中有待完善和注意的问题。     

KF-Al2O3催化下二-γ-吡喃并[2,3-a;2'''',3''''-f]萘衍生物的合成

以芳醛、氰乙酸酯和1,5-萘二酚为原料,以乙醇为溶剂,在80℃以KF/Al2O3为催化剂合成了一系列的2,8-二氨基-4,10-二芳基-4H,10H-二-γ-吡喃并[2,3-a;2',3'-f]萘-3,9-二羧酸酯衍生物,该反应具有反应条件温和、产率良好、操作方便等优点.产物的结构通过IR,1HNMR和元素分析表征,并进一步通过X射线衍射分析确证4h的结构.     

水中2-氨基-3-氰基-4-芳基-7，7-二甲基-5-氧代4H-5，6，7，8-四氢苯并[b]吡喃的洁净合成

在水溶剂中在三乙基苄基氯化铵（TEBA）存在下，取代肉桂腈与5，5-二甲基- 1，3-环已酮反应为2-氨基-3-氰基-4-芳基-7，7-二甲基-5-氧代-4H，5，6，7，8- 四氢苯并[b]吡喃提供了一种快速、方便、高效和洁净的合成方法。