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Metathesis Reactions on Solid-Phase: Towards New Synthesis Challenges

机译:固相上的易位反应:向新的合成挑战

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Today there are many types of transition-metal-catalyzed carbon-carbon bond-forming reactions. Of these, the olefin metathesis has made possible a wide range of transformations with commercially available and easily handled catalysts. Olefin metathesis is widely considered as one of the most powerful synthetic tool in organic chemistry. During the last 20 years many new catalysts with excellent selectivity and efficiency have been developed, also to be used in solid phase organic chemistry protocols. The understanding of the mechanisms and interactions between the catalyst and substrate has resulted that an increasing number of research groups have employed these reactions in multistep procedures and in the synthesis of active pharmaceutical ingredients and natural products. Although the olefin metathesis reaction still proceeds better in homogeneous phase, some structural modifications of the catalyst and new approaches for immobilization have provided interesting possibilities towards more efficient use also in heterogeneous phase. To celebrate 10 years since the Nobel Prize in Chemistry given to Yves Chauvin, Richard Schrock and Robert Grubbs for the "development of the metathesis method in organic synthesis" and to summarize recent results obtained in the field of solid phase metathesis chemistry this short review was written.
机译:如今,过渡金属催化的碳-碳键形成反应的类型很多。其中,烯烃易位使市售易处理的催化剂实现了广泛的转化。烯烃复分解被广泛认为是有机化学中最强大的合成工具之一。在过去的20年中,已经开发出许多具有优异选择性和效率的新型催化剂,也将用于固相有机化学方案中。对催化剂与底物之间机理和相互作用的理解导致越来越多的研究小组在多步程序以及活性药物成分和天然产物的合成中采用了这些反应。尽管烯烃复分解反应在均相中仍能进行得更好,但是催化剂的某些结构改性和固定化的新方法为在非均相中更有效地使用提供了有趣的可能性。为庆祝Yves Chauvin,Richard Schrock和Robert Grubbs因“有机合成中的复分解方法的发展”而获得诺贝尔化学奖十周年,并总结了在固相复分解化学领域获得的最新成果。书面。

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