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Intramolecular Stetter cyclisation of Morita-Baylis-Hillman adducts: a versatile approach towards bicycloenediones

机译:Morita-Baylis-Hillman加合物的分子内Stetter环化:双环烯二酮的通用方法

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摘要

Bicyclic enediones of various sizes can be efficiently assembled by intramolecular Stetter cyclisation of readily available Morita-Baylis-Hillman adducts. Bicyclic structures are ubiquitous subunits in a wide variety of natural products such as coronatine and guaiol (Fig. 1). The occurrence of these substructures has stimulated the development of numerous and elegant procedures for their efficient construction.
机译:通过容易获得的Morita-Baylis-Hillman加合物的分子内Stetter环化反应,可以有效地组装各种尺寸的双环烯键。双环结构是广泛的天然产物中的普遍存在的亚基,例如冠冕碱和愈创木酚(图1)。这些子结构的出现刺激了许多有效的构造方法的发展。

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