Boratyński Przemysław J, Zielińska-Błajet Mariola, Skarżewski Jacek
Department of Organic Chemistry, Wrocław University of Technology, Wrocław, Poland.
Department of Organic Chemistry, Wrocław University of Technology, Wrocław, Poland.
Alkaloids Chem Biol. 2019;82:29-145. doi: 10.1016/bs.alkal.2018.11.001. Epub 2019 Feb 22.
Major Cinchona alkaloids quinine, quinidine, cinchonine, and cinchonidine are available chiral natural compounds (chiral pool). Unlike many other natural products, these alkaloids are available in multiple diastereomeric forms which are separated on an industrial scale. The introduction discusses in short conformational equilibria, traditional separation scheme, biosynthesis, and de novo chemical syntheses. The second section concerns useful chemical applications of the alkaloids as chiral recognition agents and effective chiral catalysts. Besides the Sharpless ethers and quaternary ammonium salts (chiral PTC), the most successful bifunctional organocatalysts are based on 9-amino derivatives: thioureas and squaramides. The third section reports the main transformations of Cinchona alkaloids. This covers reactions of the 9-hydroxyl group with the retention or inversion of configuration. Specific Cinchona rearrangements enlarging [2.2.2]bicycle of quinuclidine to [3.2.2] products are connected to the 9-OH substitution. The syntheses of numerous esterification and etherification products are described, including many examples of bi-Cinchona alkaloid ethers. Further derivatives comprise 9-N-substituted compounds. The amino group is introduced via an azido function with the inversion of configuration at the stereogenic center C9. The 9-epi-amino-alkaloids provide imines, amides, imides, thioureas, and squaramides. The syntheses of 9-carbon-, 9-sulfur-, and 9-selenium-substituted derivatives are discussed. Oxidation of the hydroxyl group of any alkaloid gives ketones, which can be selectively reduced, reacted with Grignard reagents, or subjected to the Corey-Chaykovsky reaction. The alkaloids were also partially degraded by splitting C4'-C9 or N1-C8 bonds. In order to immobilize Cinchona alkaloids the transformations of the 3-vinyl group were often exploited. Finally, miscellaneous functionalizations of quinuclidine, quinoline, and examples of various metal complexes of the alkaloids are considered.
主要的金鸡纳生物碱奎宁、奎尼丁、辛可宁和辛可尼定都是手性天然化合物(手性源)。与许多其他天然产物不同,这些生物碱有多种非对映体形式,可进行工业化规模的分离。引言部分简要讨论了构象平衡、传统分离方案、生物合成和从头化学合成。第二部分涉及生物碱作为手性识别剂和有效手性催化剂的有用化学应用。除了夏普莱斯醚和季铵盐(手性相转移催化剂)外,最成功的双功能有机催化剂是基于9-氨基衍生物:硫脲和方酰胺。第三部分报道了金鸡纳生物碱的主要转化反应。这包括9-羟基的构型保持或翻转的反应。特定的金鸡纳重排反应将奎宁环的[2.2.2]双环扩大为[3.2.2]产物,这与9-OH取代有关。描述了许多酯化和醚化产物的合成,包括许多双金鸡纳生物碱醚的例子。进一步的衍生物包括9-N-取代化合物。氨基通过叠氮官能团引入,在立体中心C9处构型翻转。9-表-氨基生物碱可提供亚胺、酰胺、酰亚胺、硫脲和方酰胺。讨论了9-碳、9-硫和9-硒取代衍生物的合成。任何生物碱的羟基氧化都生成酮,酮可被选择性还原、与格氏试剂反应或进行科里-柴科夫斯基反应。生物碱也可通过断裂C4'-C9或N1-C8键进行部分降解。为了固定金鸡纳生物碱,常常利用3-乙烯基的转化反应。最后,考虑了奎宁环、喹啉的各种官能化以及生物碱的各种金属配合物的例子。