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国家自然科学基金(29972016)

作品数:7 被引量:23H指数:3
相关作者:王锐达朝山王恒山粟武杨晓武更多>>
相关机构:兰州大学中国科学院更多>>
发文基金:国家自然科学基金甘肃省自然科学基金甘肃科技攻关项目更多>>
相关领域:理学医药卫生生物学化学工程更多>>

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7 条 记 录,以下是 1-7
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光活性1,1-联萘酚(BINOL)的不对称合成被引量:5
2000年
Experimental results are reported for the CuCl2-mediated asymmetric oxidative coupling of 2-naphthols in the presence of [-]α-methylbenzylamine to optically active (S)-(-)-1,1-bi-2-naphthol. Under anhydrous conditions and with a 3∶1 molarity ratio of α-methylbenzylamine to 2-naphthol, a fair enantioselection has been observed(up to 80.6% ee).
粟武王恒山达朝山王锐
关键词:苯乙胺
内吗啡肽及其类似物的构效关系被引量:3
2000年
对内吗啡肽(endomorphins, EMs)和合理替换其2-/3-位氨基酸(amino acid, Aa)而得到的8个类似物进行了受体结合作用、 镇痛活性和舒血管效应研究, 探讨了EMs的构效关系. 结果表明: 相对而言, 2-Aa与EMs的选择性更相关, 而3-Aa则与其亲和性更相关; EMs及其类似物的镇痛和舒血管效应不完全由它们的受体结合作用(in vitro)所决定, [D-Pro2]EM-2作用独特; EMs在中枢系统中的镇痛作用和在循环系统中的舒血管作用的失活机制是不同的, 前者可能与降解有关, 而后者可能与反馈抑制有关.
霍笑风吴宁任维华王锐
关键词:内吗啡肽构效关系镇痛失活机制
The effects of the synthetic nocistatin on blood vessel activities被引量:2
2001年
Nocistatin was synthesized by the solid-phase peptide synthesis method. Its effects on rat systemic arterial pressure; rat hindquarter vascular bed resistance; tension of rabbit pectoral, abdominal, femoral aorta muscle strips without endothelium; and nociceptin induced decreases of rat systemic arterial pressure were determined. The results showed that nocistatin can increase the systemic arterial pressure, increase the hindquarter vascular bed resistance and induce the contraction significantly of abdominal, femoral aorta muscle strips without endotheiium; it has no significant effect on tension of pectoral aorta muscle strips, it cannot antagonize significantly the decrease of rat systemic arterial pressure induced by nociceptin. These results suggest that nocistatin has some important effects on blood vessel activities.
Qiang ChenYong ChenLixiang ChenDingjian YangShouliang DongRui Wang
关键词:SOLID-PHASEPOLYPEPTIDENOCISTATINNOCICEPTINSYSTEMICBLOODBLOOD
维生素B_(12)环B酰亚胺前体及琥珀胺类药物不对称合成的研究被引量:1
2000年
从γ-丁内酯合成了维生素 B1 2 环 B酰亚胺前体及琥珀酰胺类药物的 3个衍生物 ,进行了其中不对称季碳的构筑 ,改进了 Ti Cl3还原硝基乙烯类化合物的反应 。
王恒山贾强杨晓武王锐
关键词:维生素B12
树脂固定化手性联萘酚-钛催化剂的合成及其催化特性研究被引量:4
2000年
A new polymer supported BINOL ligand(4) was prepared by means of anchoring binaphthyl molecule(3) to aminoethylated polystyrene through a procedure of solid phase peptide synthesis. The key compound ( R ) 2,2 dihydroxy 1,1 binaphthyl 3 carboxylic acid(3) was prepared from R BINOL by protection of hydroxyl groups and then reaction with n butyllithium followed by carboxylation. By controlling the amount of BuLi, (3) was obtained in 55% overall yield. Ligand (4) was prepared through condensation of (3) with aminoethylated polystyrene in the presence of DCC and HOBt and found to have a loading of 0.40 mmol/g (by mass increase). The linkage between binaphthyl and aminoethylated polystyrene was indicated by a new absorption in IR spectrum of (4) at 1 644 cm -1 in comparing with what of the polystyrene. By mixing (4) with Ti(OiPr) 4 in dry CH 2Cl 2, a complex was easily prepared and this complex was found to be an efficient heterogeneous catalyst in asymmetric addition of diethylzinc to aldehydes. Optical active alcohols with up to 82% ee were obtained from the asymmtric addition with high chemical yields when 20% of (4) was used. And when benzaldehyde was used as substrate, we found that enantioselectivity increased obviously when the amount of (4) used in reaction increased from 5% to 20%;decreased the load of BINOL in ligand (4) reduced the ee of addition product; and R form of products was resulted. [WT5HZ]
王恒山粟武刘大学杨晓武达朝山王锐
关键词:不对称加成反应
手性联萘酚锂盐催化下三甲基硅氰与芳香醛的对映选择加成反应研究被引量:6
2001年
A series of aromatic cyanohydrins and their O silyl ethers have been synthesized by trimethylsilylcyanation of aromatic aldehydes using a catalyst generated in situ from optically active R (+) 1,1 2 bisnaphthol with n butyl lithium. Mandelonitrile was prepared in an isolated yield 70% with more than \{e.e.\} =60%. The effect of solvents and the amount of catalyst on enantioselectivity was also investigated.
刘大学汪权张立臣达朝山王锐
关键词:芳香醛加成反应催化剂催化活性
新的含大体积取代基的β-氨基醇配体的合成及在二乙基锌对芳香醛的不对称加成反应中的应用被引量:3
2004年
以L 脯氨酸为起始原料 ,两个在其羟基所在的α C上具有大体积取代基的 β 氨基醇配体被简便地合成出来 ,并被用于催化二乙基锌对醛的不对称加成 ,得到了ee值较高的S构型的手性二级醇 .
达朝山辛卓群肖亦男王恒山粟武杨帆王锐
关键词:二乙基锌芳香醛不对称加成反应取代基L-脯氨酸手性醇
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