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Michael addition-based cyclization strategy in the total synthesis of Lycopodium alkaloids
Michael addition-based cyclization strategy in the total synthesis of Lycopodium alkaloids
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Michael addition-based cyclization strategy in the total synthesis of Lycopodium alkaloids
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Michael addition-based cyclization strategy in the total synthesis of Lycopodium alkaloids
Michael addition-based cyclization strategy in the total synthesis of Lycopodium alkaloids

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Michael addition-based cyclization strategy in the total synthesis of Lycopodium alkaloids
Michael addition-based cyclization strategy in the total synthesis of Lycopodium alkaloids
Journal Article

Michael addition-based cyclization strategy in the total synthesis of Lycopodium alkaloids

2016
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Overview
Lycopodium alkaloids, a unique family of biologically important natural products isolated and characterized from various species ofLycopodium (sensu lato), have attracted extensive attention from chemists and pharmacists in the past three decades. Michael addition-based cyclization has been successfully employed as an elegant and efficient ring-construction protocol of constructing key cyclohexanone intermediates in the total synthesis of Lycopodium alkaloids. This mini-review chooses and summarizes several representative total syntheses of various Lycopodium alkaloids in which intramolecular Michael addition severed as the key methodology.