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Subsequently,enol methylation of P in basic condition completed the synthesis of malyngamide O.Applied this route to the synthesis of malyngamides Q and R,the chiral unsaturated acid was connected with the vinyl chloride part by amidation,then the resulting product was converted into the corresponding aldehyde,followed by aldol condensation of the aldehyde with the chlorotitanium enolate of pyrrolidone to complete the skeleton of malyngamides Q and R,then the synthesis of them was completed via enol methylation in acid condition.

该合成路线拓展应用到malyngamides Q和R的合成时,首先用酰胺键将手性不饱和脂肪酸和烯氯片段连接,再转化成相应的醛,与乙酰基吡咯酮进行TiCl_4催化的aldol反应即得到malyngamides Q和R的骨架结构,再经过酸催化的烯醇甲基化反应完成了Q和R的全合成。

Methods: The model of evaluating T cell proliferation stimulated with polyclonal activators, ConA was established by vital dye carboxyl fluorescin diacetate succinmidyl ester labeling technique. The effect of a specific inhibitor for p38 MAPK, SB253580, on T cell proliferation on different doses and in different time was estimated by flow cytometry. At the same time, the percentage of proliferating T cells and proliferation index were measured by CellQuest and SPSS10.0 for Windows softwares.

以活体染料羧基荧光素乙酰乙酸琥珀酰亚胺酯染色,建立了在多克隆刺激剂刀豆蛋白A刺激下评价小鼠T细胞增殖的模型,通过流式细胞术分析p38丝裂原活化蛋白激酶的特异性抑制剂SB203580在不同剂量、不同时间对T细胞增殖的作用,并应用CellQuest和SPSS10.0 for Windows软件分析增殖细胞各代所占比例和增殖指数。

Methods: A model to evaluate lymphocyte proliferation stimulated with a polyclonal activator, concanavalin A, was established by vital dye carboxyl fluorescin diacetate succinmidyl ester labeling technique. Effects of the different doses of anisomycin on the lymphocyte proliferation were estimated by flow cytometry and MTT methods. The propidium iodide labeling technique was applied to assay the effect of the different doses of anisomycin on changes of the lymphocyte cell-cycle stimulated by ConA or by phorbol ester plus Ionomycin. The percentage of the expression level of CD69 and CD25 on the activated lymphocytes was evaluated by fluorescin-conjugated monoclonal antibody double labeling technique.

以活体染料羧基荧光素乙酰乙酸琥珀酰亚胺酯染色,建立在多克隆刺激剂刀豆蛋白A刺激下评价小鼠淋巴细胞增殖的模型,通过流式细胞术和MTT法分析茴香霉素在不同剂量下对淋巴细胞增殖的作用;采用碘化丙锭染色分析茴香霉素对ConA或佛波醇酯加离子霉素刺激的小鼠淋巴细胞周期变化的作用;利用荧光标记的单克隆抗体双染技术和流式细胞术观察茴香霉素对小鼠CD3~+T细胞早期及中期活化标志分子CD69和CD25表达的影响。

Experiments show the maximum absorption wavelength of 1,1 diactyl ferrocene and 1,1 DiN, N glucosan...

测定了 1 ,1 -二乙酰基二茂铁、葡胺糖丙酰二茂铁的最大吸收波长,分别是 45 6nm和 346nm。

In the forth part, the heterotactic enthalpic pairwise interaction coefficients between five amides and butanediol isomers (1,3-butanediol, 1,4-butanediol and 2,3-butanediol) at 310.15K are discussed. The change of temperature made remarkable effects on the values of h_.

第四部分:经测定得到了五种酰胺与丁二醇的三种异构体在298.15K(25℃)时的各级异系焓相互作用系数,并进行了分析比较,讨论了五种乙酰胺分子与三种丁二醇分子的相互作用机制。

The reaction of chiral isocyanide with N-sulfonylimine catalyzed byRh complex gave 2-imidazoline in 68 - 82% diastereoselectivity.

本论文由五部分组成·在没有任何酸,碱和催化剂存在下, N-磺酰亚胺与异氰乙酰胺反应,以60-94%的产率生成1,3-恶唑。1,3-恶唑的结构由X-ray分析测定。

Results Ginsenosides were produced from esterolysis of corresponding malonyl ginsenosides in red ginseng processing.

结果在红参加工过程中丙二酸单酰人参皂苷酯键水解产生相应的人参皂苷,脱羧产生相应的糖乙酰化人参皂苷。

Results Ginsenosides were produced from esterolysis of corresponding malonyl ginsenosides in red ginseng processing. Another reaction of malonyl ginsenosides in red ginseng processing was decarboxylated to produce corresponding acetyl ginsenosides.

结果在红参加工过程中丙二酸单酰人参皂苷酯键水解产生相应的人参皂苷,脱羧产生相应的糖乙酰化人参皂苷。

The intermediate which obtained from oximation of 7a-e reacted withmethyl N-(2-bromomethylphenyl)-N-methoxycarbamate to synthesize oxime ether methyl carbamate 3a-e.

以邻位卤代苯甲醛和3-丁烯-2-醇为原料通过钯催化&一锅法&反应合成了2-乙酰基茚7a-e,7a-e 肟化之后和N-(2-溴甲基苯基)-N-甲氧基氨基甲酸甲酯反应合成了肟醚类氨基甲酸甲酯3a-e,进一步胺解之后得到了肟醚类氨基甲酰甲胺3f-j。

In thesecond chapter, eleven 1,3,4-oxadizoles bearing chiral pyrazolyl moieties(4a-k) andfive triazolotriazines bearing chiral pyrazolyl moieties(5a-e) were obtained from5-[(1"S)-1",2-diacetyl-oxyethyl]-1-phenylpyrazol-3-carboxaldehyde(1) with arylcar-bohydrazide or (5-aryl-1,2,4-triazin-3-yl)hydrazine through an intramolecular1,3-dipolar cycloaddition in the presence of the non-metal oxidant IBD.

其中第二章介绍了以D-葡萄糖为原料制得的5-[(1′S)-1′,2′-二乙酰氧基乙基]-1-苯基吡唑-3-醛(1)分别与芳基甲酰肼、(5-取代苯基-1,2,4-三嗪-3-基)肼反应,在无金属氧化剂—IBD引发下,发生分子内1,3-偶极环加成,采用&一锅煮&法合成了11种含手性吡唑基的1,3,4-噁二唑类化合物(4a-k)和5种含手性吡唑基的三唑并三嗪类化合物(5a-e)。

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