Kirschning Andreas, Monenschein Holger, Wittenberg Rüdiger
Institut für Organische Chemie Universität Hannover Schneiderberg 1B, 30167 Hannover (Germany).
Angew Chem Int Ed Engl. 2001 Feb 16;40(4):650-679.
As part of the dramatic changes associated with the need for preparing compound libraries in pharmaceutical and agrochemical research laboratories, industry searches for new technologies that allow for the automation of synthetic processes. Since the pioneering work by Merrifield polymeric supports have been identified to play a key role in this field however, polymer-assisted solution-phase synthesis which utilizes immobilized reagents and catalysts has only recently begun to flourish. Polymer-assisted solution-phase synthesis has various advantages over conventional solution-phase chemistry, such as the ease of separation of the supported species from a reaction mixture by filtration and washing, the opportunity to use an excess of the reagent to force the reaction to completion without causing workup problems, and the adaptability to continuous-flow processes. Various strategies for employing functionalized polymers stoichiometrically have been developed. Apart from reagents that are covalently or ionically attached to the polymeric backbone and which are released into solution in the presence of a suitable substrate, scavenger reagents play an increasingly important role in purifying reaction mixtures. Employing functionalized polymers in solution-phase synthesis has been shown to be extremely useful in automated parallel synthesis and multistep sequences. So far, compound libraries containing as many as 88 members have been generated by using several polymer-bound reagents one after another. Furthermore, it has been demonstrated that complex natural products like the alkaloids (+/-)-oxomaritidine and (+/-)-epimaritidine can be prepared by a sequence of five and six consecutive polymer-assisted steps, respectively, and the potent analgesic compound (+/-)-epibatidine in twelve linear steps ten of which are based on functionalized polymers. These developments reveal the great future prospects of polymer-assisted solution-phase synthesis.
作为制药和农用化学品研究实验室中与制备化合物库的需求相关的巨大变革的一部分,工业界在寻找能够实现合成过程自动化的新技术。自梅里菲尔德的开创性工作以来,聚合物载体已被确定在该领域发挥关键作用,然而,利用固定化试剂和催化剂的聚合物辅助溶液相合成直到最近才开始蓬勃发展。聚合物辅助溶液相合成相对于传统溶液相化学具有多种优势,例如通过过滤和洗涤易于从反应混合物中分离负载的物种,有机会使用过量的试剂促使反应完全进行而不会引起后处理问题,以及对连续流动过程的适应性。已经开发了多种化学计量使用功能化聚合物的策略。除了共价或离子连接到聚合物主链并在合适底物存在下释放到溶液中的试剂外,清除剂在纯化反应混合物中发挥着越来越重要的作用。在溶液相合成中使用功能化聚合物已被证明在自动化平行合成和多步序列中非常有用。到目前为止,通过依次使用几种聚合物结合试剂已经生成了多达88个成员的化合物库。此外,已经证明,复杂的天然产物如生物碱(±)-氧代马里替丁和(±)-表马里替丁可以分别通过五个和六个连续的聚合物辅助步骤制备,而强效镇痛化合物(±)-埃博霉素可以通过十二个线性步骤制备,其中十个步骤基于功能化聚合物。这些进展揭示了聚合物辅助溶液相合成的巨大未来前景。