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Selective probes for nicotinic acetylcholine receptros from substituted AE-bicyclic analogs of methyllycacontine

机译:来自甲基甘草精的取代AE-双环类似物的烟碱乙酰胆碱受体的选择性探针

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摘要

A concise,kpractical approach to substituted [3.3.1]-AE-bicyclic analogs of methyllycaconitine (MLA) has bene developed employing dianion alkylation and double Mannich reactions.Acetylide anion addition to substituted cyclohexanones and manipulaiton of the acetylide alkoxide dianion genrates sueful bis-propargyl tertiary alcohols.The design adn synthesis of probes for nicotinic acetylcholine receptros (nAChR) affords possible leads for pesticides.MLA also has potential inporbing neuronal nAChR which are implicated in some metchanisms of neurodegeneration.
机译:一种简单,实用的方法,是通过使用二价阴离子烷基化和双重曼尼希反应,开发了取代的[3.3.1] -AE-双环甲基甘可耐碱(MLA)类似物。取代环己酮中乙二醛阴离子的加成和乙炔醇氧基化物二阴离子的手性产生可疑的双-烟酸乙酰胆碱受体(nAChR)探针的设计和合成为农药提供了可能的线索。MLA还具有潜在侵入神经元nAChR的能力,这与某些神经退行性机制有关。

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