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Synthesis of functionalized macrocycles by ring closing metathesis

机译:闭环易位合成功能化大环

摘要

The invention concerns an improved process for the preparation of macrocyclic products with 12 or more ring atoms containing one or more polar functional groups on the ring and/or one or more heteroatoms within the ring by ring closing metathesis (RCM) of suitably substituted diene precursors even if the substrates are devoid of any kind of conformational preorganization. Metal carbene complexes of Ru, Mo, W, Re, Os, which are tolerant towards the respective functional group and can either be isolated or prepared in situ are used as catalysts or catalyst precursors. Preferred catalysts or catalyst precursors are ruthenium complexes of the general type XX.sub.1 LL.sub.1 Ru═CRR.sub.1, wherein X, X.sub.1 =halogen, L, L.sub.1 =trialkylphosphine, R, R1=H, Ph, CH═ CPh.sub.2 denote the most preferred embodiment. The process can be applied to the synthesis of olfactory compounds, perfumary ingredients, pheromones, crown ethers, antibiotics and pharmaceuticals for human and veterinary medicine.
机译:本发明涉及一种通过适当取代的二烯前体的闭环复分解(RCM)制备具有12个或更多个环原子的大环产物的改进方法,所述大环产物在环上含有一个或多个极性官能团和/或在环内具有一个或多个杂原子。即使底物没有任何种类的构象预组织。 Ru,Mo,W,Re,Os的金属卡宾配合物可耐受相应的官能团,并且可以分离或原位制备,用作催化剂或催化剂前体。优选的催化剂或催化剂前体是一般XX.sub.1 LL.sub.1 Ru═ CRR.sub.1的钌配合物,其中X,X.sub.1 =卤素,L,L.sub.1 =三烷基膦,R,R1 = H,Ph,CH═ CPh.sub.2表示最优选的实施例。该方法可用于合成嗅觉化合物,香水成分,信息素,冠醚,抗生素以及用于人类和兽医学的药物。

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