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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。

Compared with theoretical values 49.0%C,7.8%H,17.1%N the elemental analysis results of YXA2.3 that was 45.1%C,4.7%H and 11.1%N showed that oxycellulose chloride were aminated only partially in about 45%yield because of their huge molecular volume.

对YXA2.3进行有机元素分析结果为：C 45.1，H 4.7，N 11.1(理论值为：C 49.0，H 7.8，N 17.1)，其中11.1＜17.1，4.7＜7.8，这是由于大分子的特性，氧化纤维素的氯化物只部分发生的胺化。

Acrylic resin containing N,N-dimethyl amino group and vinyl group applicable for UV-curable and cathodic electrophoretic paint was synthesized via radical polymerization of acrylic monomers followed by modification with methacrylic oxyethyl isocyanate.

通过自由基共聚合得到丙烯酸树脂，然后用甲基丙烯酸异氰酸乙酯对其改性，合成了既带有N，N-二甲胺基，又带有乙烯基的紫外光固化阴极电泳漆基体树脂。

In order to check the corresponding compound at 31P NMR –45.4 ppm, stable pentacoordinate spirobicyclic 2-phenoxy-1,3-phenylene-dioxo-1,3,2-iminoacetoxyphosphoranes were synthesized through a new and efficient method whereby phosphorus pentachloride was displaced stepwise by catechol, N,O-bisamino acid and phenol, or catechol, phenol and N,O-bisamino acid, their 31P NMR chemical shifts are at about 31P NMR –45.0 ppm, the results showed that the compound 4 at 31P NMR –45.4 ppm was pentacoordinate phosphorane containing amino acid residue.

采用磷谱跟踪来研究上述成肽反应机理。例如在氮气保护下，0.1mmol O，O-亚苯基磷酰氯（1）和0.15mmol N，O-二苯丙氨酸（2）苯溶液加入0.6ml核磁管中，混合均匀，反应过程用磷谱检测。反应1分钟后，起始原料1(δp=19ppm)很快转变成N-磷酰苯丙氨酸的三甲基硅基酯（3）(δp=19.8ppm)，在8分钟内，3完全转变成苯丙氨酸磷烷4(δp =-45.4ppm)，同时出现环磷三酯（6）(δp=3.5ppm)。随着反应的进行，对应于化合物4的峰逐渐变小，而6逐渐变大。

Cu2-Co2-KBr with high catalytic activity and selectivity shows synergistic effect between metal ions.Under the reaction conditions of mCu(Ac2:mCo(Ac2:m= 0.1:0.5:0.1, n:n=0.14, glacial acetic acid as solvent, overdosage sodium percarbonate, 65℃, the conversion can reach 45.9% and the selectivity for p-methoxy benzaldhyde is about 68.3%.

结果表明，Cu2-Co2-KBr具有较高的催化活性和选择性，体现出金属离子之间的协同作用，对甲基苯甲醚在mCu(Ac2：mCo(Ac2：m=0.1：0.5：0.1，n：n=0.14，冰醋酸作溶剂，稍过量的过碳酸钠，65℃的条件下，转化率可达45.9%，生成对甲氧基苯甲醛的选择性为68.3%。

Pilot-plant test for synthesis of poly/attapulgite superabsorbent composite was carried out using acrylic acid and attapulgite as main raw materials,N,N′-methylene-bisacrylamide as crosslinker and composite composed of V-50 and ammonium persulphate as initiator by solution polymerization in a 100 L pilot-plant test equipment.

在100 L的中试设备上，用水溶液聚合法，以丙烯酸和凹凸棒黏土为主要原料，以N，N-亚甲基双丙烯酰胺为交联剂，V-50和过硫酸钾复配作为引发体系，进行了聚丙烯酸/凹凸棒复合保水剂的中试放大实验。

Study on Extender N,N-Di(2-hydroxypropyl) phenylamine

扩链剂N，N-二(2-羟丙基)苯胺的研究

Synthesis of Organic Pigmet Intermidiate N, N'- bisacetylaceto - 2 - methyl - 5 - chloro -1,4- Phenylenediamine

有机颜料中间体N，N′-双乙酰乙酰基2-甲基-5-氯代-1，4-苯二胺的合成

Gabriel reaction was adopted to synthesis 2-(0ctahydro-1-azocinyl)ethylamine, N-(β-Heptamethyleniminoethy1)phthalimide was prepared by treating Heptamethylenimine with N -(β-bromoethy1) phthalimide. N -(β-bromoethy1) phthalimide was easily prepared from phthalic anhydride in two steps.

我们采用Gabriel伯胺合成法制备2-环庚亚胺基乙胺，从邻苯二甲酸酐经过两步反应很容易地得到N-邻苯二甲酰亚胺，然后与环庚亚胺发生亲核取代反应，产物再水解制得伯胺2-环庚亚胺基乙胺。

N-propyl-4-(N-methylacryloxy-ethyl)amino-1,8-naphthalimide was synthesized and used for determination of picric acid.

合成了N-丙基-4-(N-甲基丙烯酰基氧乙基)氨基-1，8-萘酰亚胺，研制出了苦味酸荧光光纤传感器，可间接测定药片中磷酸氯喹和水样中苦味酸的含量。

And Pharaoh spoke to Joseph, saying, Your father and your brothers have come to you.

47：5 法老对约瑟说，你父亲和你弟兄们到你这里来了。

Additionally, the approximate flattening of surface strip using lines linking midpoints on perpendicular lines between geodesic curves and the unconditional extreme value method are discussed.

提出了用测地线方程、曲面上两点间短程线来计算膜结构曲面测地线的方法，同时，采用测地线间垂线的中点连线和用无约束极值法进行空间条状曲面近似展开的分析。