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1)  Cinchona alkaloid
金鸡纳碱
1.
The applications of cinchona alkaloids and parts of their derivatives in asymmetric synthesis were reviewed with 34 references.
综述了近年来金鸡纳碱及其部分衍生物在不对称合成中的应用。
2.
In our work,we changed the pore sizes of the nanoporous supports and introduce cinchona alkaloid in the nanopores.
本文通过调变介孔氧化硅材料载体的孔径尺寸构建了具有不同限域空间的多相金鸡纳碱手性催化剂。
2)  Cinchona alkaloids
金鸡纳碱
1.
2) Some cinchona-derived quaternary ammonium salts were synthesized from cinchona alkaloids, which were used as cocatalyst combined SalenCo(OAc) to catalyze the coupling reaction of epoxide and carbon dioxide.
2)我们用金鸡纳碱合成了一系列的手性季铵盐,并首次用其作共催化剂与SalenCo(OAc)催化环碳酸酯的合成,其中以氯化-N-苄基辛可宁(la)为共催化剂,在室温下环丙烯碳酸酯的ee值达到73%。
3)  4-Quinolyl(5-vinyl-1-azabicyclo[2.2.2]oct-2-yl)methanol
弱金鸡纳碱
4)  Cinchona alkaloid
金鸡纳生物碱
1.
I Synthesis of Cinchona Alkaloid Ligands II Synthesis of Derivatives of Gentiopicroside and the Antiviral Effects of Them Against Coxsackievirus B3 and Simian Immunodeficiency Virus in Vitro;
I 金鸡纳生物碱衍生物的合成方法研究 II 龙胆苦苷衍生物的合成及其对CVB3和SIV的体外抑制作用
2.
Six chiral diamine ligands were synthesized from natural Cinchona alkaloids, quinine and cinchonine, under mild conditions.
以价廉易得的天然金鸡纳生物碱奎宁和辛可宁为原料,在温和条件下容易地合成了6种手性双胺配体。
5)  cinchona alkaloids
金鸡纳生物碱
1.
Two typical examples, asymmetric hydrogenation of α, β \|ketoesters on nickel catalysts modified with tartaric acid derivatives and on platinum catalysts modified with cinchona alkaloids are introduced and discussed in detail.
特别是对最近几年来两个典型的多相不对称催化氢化体系即酒石酸盐修饰镍催化剂催化 β-酮酸酯的不对称氢化反应体系和金鸡纳生物碱修饰铂催化剂催化 α-酮酸酯的不对称氢化反应体系进行了详细的介绍和讨论 ,同时展望了多相不对称催化氢化反应研究的前景。
2.
Applications of cinchona alkaloids as chiral selectors in HPLC and CE are reviewed.
综述了金鸡纳生物碱作为手性选择剂在高效液相色谱和毛细管电泳中分离光学异构体的应用。
3.
However, in the last two decades, Cinchona alkaloids have become more attractive due to their successful applications in asymmetric synthesis.
奎宁等金鸡纳生物碱作为治疗疟疾的主要药物被人们早已熟知。
6)  cinchona alkaloid-derived ligands
金鸡纳碱衍生物
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